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Front of the Class 叫我第一名 (USA,2008)

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发表于 2013-7-25 20:38:05 | 显示全部楼层 |阅读模式
  叫我第一名 预告 中文字幕 (front of the class trailer), http://v.youku.com/v_show/id_XNTg0NDI4ODIw.html


Front of the Class 叫我第一名 / 开放有爱 / 站在教室前 / 讲台前的我
trailer 预告片http://v.youku.com/v_show/id_XNTg0NDI4ODIw.html


Brad Cohen's story starts as a young boy whose mother helped doctors to realize that he had Tourette syndrome. With his mother's help and the support of his school principal, Brad eventually becomes an award-winning teacher.

BoBo(詹姆斯•沃克 James Wolk 饰)患有先天性的妥瑞氏症,这种严重的痉挛疾病,导致他无法控制地扭动脖子和发出奇怪的声音。而这种怪异的行为,更是让他从小不被周围的人理解,在学校里老师经常批评他,同学们更是对他冷嘲热讽,就连他的父亲也对他失望透顶。只有他的母亲一直是他的坚实臂弯,母亲的坚持与鼓励,让他能够在正常人的生活里艰难前行。然而面对这个不能理解他的世界,BoBo一直在痛苦的漩涡里挣扎。直到在一次全校大会上校长在众人面前巧妙的让大家了解了BoBo的真实情况,让他有了成为一名关爱学生的教师的坚定梦想,即使因为这个病症让BoBo在寻求教师梦想的道路上遭到众人怀疑,屡屡受挫,但他始终坚持着自己的这份梦想, 为了找到一个愿意接受自己的学校,不抛弃梦想,不放弃信念,默默的努力。而他曾经曲折的人生道路在他的坚持下也开始慢慢好转…
  该片根据布拉德•科恩的真实故事改编。

Front of the Class is a 2008 American drama film based on the book by Brad Cohen, Front of the Class: How Tourette Syndrome Made Me the Teacher I Never Had, co-authored by Lisa Wysocky.
The book was made into a Hallmark Hall of Fame TV movie starring newcomer James Wolk—a 2007 University of Michigan graduate[1]—and featuring Treat Williams and Emmy Award-winning actress Patricia Heaton as Cohen's parents; the movie aired on CBS on December 7, 2008.[2]
  
Reception
Cohen was concerned that the movie should stay truthful and avoid sensationalizing Tourette syndrome. He was pleased with the overall result, although he noted some dates in his life were sped up for effect (for example, the date of his wedding).[1]
PlotTwelve-year-old Brad lives in Missouri with his divorcée mother, Ellen, and younger brother, Jeff. He constantly gets into trouble with his father Norman and his teachers at school due to his tics. In one class, his teacher calls him to the front to make him apologize to his class for disrupting the class and promise he won't do it again. Determined to find out what is wrong with her son, Ellen seeks medical help. A psychiatrist believes that Brad's tics are the result of his parents' divorce. One lady suggests an exorcism. Ellen takes her search to the library and comes across Tourette syndrome (TS) in a medical book. She show this to the psychiatrist, who agrees with the diagnosis, and says that there is no cure. Brad and his mother attend a support group for the first and last time. From then on, Brad aspires to never be like the other members of the support group and to become successful.
At the beginning of middle school, Brad is sent to the principal's office for being disruptive. The Principal invites him to the school concert later in the afternoon. At the end of the concert, he calls Brad up to the stage and asks Brad to talk about his TS. As Brad makes his way back to his seat, the school applauds him.
As an adult, Brad lives with his house mate Ron in Georgia, and is looking for work as an elementary school teacher. He is turned down after many interviews because of his TS. He finally gets an interview where the staff are accepting and they give him the job.
On his first day, Brad explains his TS to the children. He helps Thomas with reading and makes an impression on Heather, a girl with terminal cancer. One student's father pulls her out of Brad's class as he fears Brad will distract her.
Brad meets Nancy on an online dating site and invites her over for Thanksgiving back at Ellen's house, where he tells Nancy he loves her, and the feeling is reciprocated. He confides in Ellen his concern that Nancy will get fed up of his tics, but she reassures him that he mustn't let his TS get in the way.
An observer at the school assesses Brad's teaching, and the headteacher announces that Brad has been chosen to receive the Teacher of the Year award, which he accepts his award in front his family, friends and students. The ending titles tell that Brad got his Master's degree; he dressed up as Homer, the Atlanta Braves mascot; he married Nancy in 2006; and photographs of the real Brad Cohen teaching his class are shown.
 楼主| 发表于 2013-7-25 20:41:54 | 显示全部楼层
本帖最后由 Ray 于 2013-7-26 13:36 编辑


叫我第一名 Front of the class 【标清】【中英双字幕】[entire movie uploaded],   http://www.tudou.com/programs/view/sLuYG5O2RaQ/

    



















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 楼主| 发表于 2013-7-25 20:48:56 | 显示全部楼层
Tourette syndromeFrom Wikipedia, the free encyclopedia, http://en.wikipedia.org/wiki/Tourette_syndrome


Tourette syndrome (also called Tourette's syndrome, Tourette's disorder, Gilles de la Tourette syndrome, GTS or, more commonly, simply Tourette's or TS) is an inherited neuropsychiatric disorder with onset in childhood, characterized by multiple physical (motor) tics and at least one vocal (phonic) tic. These tics characteristically wax and wane, can be suppressed temporarily, and are preceded by a premonitory urge. Tourette's is defined as part of a spectrum of tic disorders, which includes provisional, transient and persistent (chronic) tics.
Tourette's was once considered a rare and bizarre syndrome, most often associated with the exclamation of obscene words or socially inappropriate and derogatory remarks (coprolalia), but this symptom is present in only a small minority of people with Tourette's.[1] Tourette's is no longer considered a rare condition, but it is not always correctly identified because most cases are mild and the severity of tics decreases for most children as they pass through adolescence. Between 0.4% and 3.8% of children ages 5 to 18 may have Tourette's;[2] the prevalence of other tic disorders in school-age children is higher, with the more common tics of eye blinking, coughing, throat clearing, sniffing, and facial movements. Extreme Tourette's in adulthood is a rarity, and Tourette's does not adversely affect intelligence or life expectancy.
Genetic and environmental factors play a role in the etiology of Tourette's, but the exact causes are unknown. In most cases, medication is unnecessary. There is no effective treatment for every case of tics, but certain medications and therapies can help when their use is warranted. Education is an important part of any treatment plan, and explanation and reassurance alone are often sufficient treatment.[1][3] Comorbid conditions (co-occurring diagnoses other than Tourette's) such as attention-deficit hyperactivity disorder (ADHD) and obsessive–compulsive disorder (OCD) are present in many patients seen in tertiary specialty clinics. These other conditions often cause more functional impairment to the individual than the tics that are the hallmark of Tourette's, hence it is important to correctly identify comorbid conditions and treat them.[4]
The eponym was bestowed by Jean-Martin Charcot (1825–1893) on behalf of his resident, Georges Albert Édouard Brutus Gilles de la Tourette (1859–1904), a French physician and neurologist, who published an account of nine patients with Tourette's in 1885.

Georges Gilles de la Tourette (1857–1904), namesake of Tourette syndrome
Classification

Tics are sudden, repetitive, nonrhythmic movements (motor tics) and utterances (phonic tics) that involve discrete muscle groups.[5] Motor tics are movement-based tics, while phonic tics are involuntary sounds produced by moving air through the nose, mouth, or throat.
Tourette's was classified by the fourth version of the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-TR) as one of several tic disorders "usually first diagnosed in infancy, childhood, or adolescence" according to type (motor or phonic tics) and duration (transient or chronic). Transient tic disorders consisted of multiple motor tics, phonic tics or both, with a duration between four weeks and twelve months. Chronic tic disorder was either single or multiple, motor or phonic tics (but not both), which were present for more than a year.[5] Tourette's (DSM-IV 307.23) is diagnosed when multiple motor tics, and at least one phonic tic, are present for more than a year.[6] The fifth version of the DSM (DSM-5), published in May 2013, reclassified Tourette's and tic disorders as motor disorders listed in the neurodevelopmental disorder category, and replaced transient tic disorder with provisional tic disorder, but made few significant other changes.[7][8][9]
Tic disorders are defined only slightly differently by the World Health Organization International Statistical Classification of Diseases and Related Health Problems, ICD-10; code F95.2 is for combined vocal and multiple motor tic disorder [de la Tourette].[10]
Although Tourette's is the more severe expression of the spectrum of tic disorders,[11] most cases are mild.[2] The severity of symptoms varies widely among people with Tourette's, and mild cases may be undetected.[5]
Characteristics

Examples of motor tics


Tics are movements or sounds "that occur intermittently and unpredictably out of a background of normal motor activity",[12] having the appearance of "normal behaviors gone wrong".[13] The tics associated with Tourette's change in number, frequency, severity and anatomical location. Waxing and waning—the ongoing increase and decrease in severity and frequency of tics—occurs differently in each individual. Tics also occur in "bouts of bouts", which vary for each person.[5]
Coprolalia (the spontaneous utterance of socially objectionable or taboo words or phrases) is the most publicized symptom of Tourette's, but it is not required for a diagnosis of Tourette's and only about 10% of Tourette's patients exhibit it.[1] Echolalia (repeating the words of others) and palilalia (repeating one's own words) occur in a minority of cases,[5] while the most common initial motor and vocal tics are, respectively, eye blinking and throat clearing.[14]
In contrast to the abnormal movements of other movement disorders (for example, choreas, dystonias, myoclonus, and dyskinesias), the tics of Tourette's are temporarily suppressible, nonrhythmic, and often preceded by an unwanted premonitory urge.[15] Immediately preceding tic onset, most individuals with Tourette's are aware of an urge,[16][17] similar to the need to sneeze or scratch an itch. Individuals describe the need to tic as a buildup of tension, pressure, or energy[17][18] which they consciously choose to release, as if they "had to do it"[19] to relieve the sensation[17] or until it feels "just right".[19][20] Examples of the premonitory urge are the feeling of having something in one's throat, or a localized discomfort in the shoulders, leading to the need to clear one's throat or shrug the shoulders. The actual tic may be felt as relieving this tension or sensation, similar to scratching an itch. Another example is blinking to relieve an uncomfortable sensation in the eye. These urges and sensations, preceding the expression of the movement or vocalization as a tic, are referred to as "premonitory sensory phenomena" or premonitory urges. Because of the urges that precede them, tics are described as semi-voluntary or "unvoluntary",[12] rather than specifically involuntary; they may be experienced as a voluntary, suppressible response to the unwanted premonitory urge.[1] Published descriptions of the tics of Tourette's identify sensory phenomena as the core symptom of the syndrome, even though they are not included in the diagnostic criteria.[18][21][22]
Video clips of tics

While individuals with tics are sometimes able to suppress their tics for limited periods of time, doing so often results in tension or mental exhaustion.[1][4] People with Tourette's may seek a secluded spot to release their symptoms, or there may be a marked increase in tics after a period of suppression at school or at work.[13] Some people with Tourette's may not be aware of the premonitory urge. Children may be less aware of the premonitory urge associated with tics than are adults, but their awareness tends to increase with maturity.[12] They may have tics for several years before becoming aware of premonitory urges. Children may suppress tics while in the doctor's office, so they may need to be observed while they are not aware they are being watched.[23] The ability to suppress tics varies among individuals, and may be more developed in adults than children.
Although there is no such thing as a "typical" case of Tourette syndrome,[24] the condition follows a fairly reliable course in terms of the age of onset and the history of the severity of symptoms. Tics may appear up to the age of eighteen, but the most typical age of onset is from five to seven.[5] A 1998 study published by Leckman et al. of the Yale Child Study Center[25] showed that the ages of highest tic severity are eight to twelve (average ten), with tics steadily declining for most patients as they pass through adolescence.[20] The most common, first-presenting tics are eye blinking, facial movements, sniffing and throat clearing. Initial tics present most frequently in midline body regions where there are many muscles, usually the head, neck and facial region.[24] This can be contrasted with the stereotyped movements of other disorders (such as stims and stereotypies of the autism spectrum disorders), which typically have an earlier age of onset, are more symmetrical, rhythmical and bilateral, and involve the extremities (e.g., flapping the hands).[26] Tics that appear early in the course of the condition are frequently confused with other conditions, such as allergies, asthma, and vision problems: pediatricians, allergists and ophthalmologists are typically the first to see a child with tics.[5]
Among patients whose symptoms are severe enough to warrant referral to clinics, obsessive–compulsive disorder (OCD) and attention-deficit hyperactivity disorder (ADHD) are often associated with Tourette's.[20] Not all persons with Tourette's have ADHD or OCD or other comorbid conditions, although in clinical populations, a high percentage of patients presenting for care do have ADHD.[20][27] One author reports that a ten-year overview of patient records revealed about 40% of patients with Tourette's have "TS-only" or "pure TS", referring to Tourette syndrome in the absence of ADHD, OCD and other disorders.[28][29] Another author reports that 57% of 656 patients presenting with tic disorders had uncomplicated tics, while 43% had tics plus comorbid conditions.[13] People with "full-blown Tourette's" have significant comorbid conditions in addition to tics.[13]
CausesMain article: Causes and origins of Tourette syndrome
The exact cause of Tourette's is unknown, but it is well established that both genetic and environmental factors are involved.[30] Genetic epidemiology studies have shown that the overwhelming majority of cases of Tourette's are inherited, although the exact mode of inheritance is not yet known and no gene has been identified.[4][31][32] In other cases, tics are associated with disorders other than Tourette's, a phenomenon known as tourettism.[33]
A person with Tourette's has about a 50% chance of passing the gene(s) to one of his or her children, but Tourette's is a condition of variable expression and incomplete penetrance.[34] Thus, not everyone who inherits the genetic vulnerability will show symptoms; even close family members may show different severities of symptoms, or no symptoms at all. The gene(s) may express as Tourette's, as a milder tic disorder (provisional or chronic tics), or as obsessive–compulsive symptoms without tics. Only a minority of the children who inherit the gene(s) have symptoms severe enough to require medical attention.[35] Gender appears to have a role in the expression of the genetic vulnerability: males are more likely than females to express tics.[23]
Non-genetic, environmental, post-infectious, or psychosocial factors—while not causing Tourette's—can influence its severity.[24] Autoimmune processes may affect tic onset and exacerbation in some cases. In 1998, a team at the US National Institute of Mental Health proposed a hypothesis based on observation of 50 children that both obsessive–compulsive disorder (OCD) and tic disorders may arise in a subset of children as a result of a poststreptococcal autoimmune process.[2] Children who meet five diagnostic criteria are classified, according to the hypothesis, as having Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal infections (PANDAS).[36] This contentious hypothesis is the focus of clinical and laboratory research, but remains unproven.[1][2][37]
Some forms of OCD may be genetically linked to Tourette's.[20][38] A subset of OCD is thought to be etiologically related to Tourette's and may be a different expression of the same factors that are important for the expression of tics.[39] The genetic relationship of ADHD to Tourette syndrome, however, has not been fully established.[29]
Pathophysiology
Brain structures implicated in Tourette syndrome


The exact mechanism affecting the inherited vulnerability to Tourette's has not been established, and the precise etiology is unknown. Tics are believed to result from dysfunction in cortical and subcortical regions, the thalamus, basal ganglia and frontal cortex.[30] Neuroanatomic models implicate failures in circuits connecting the brain's cortex and subcortex,[24] and imaging techniques implicate the basal ganglia and frontal cortex.[31]
Diagnosis
According to the revised fourth edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-TR), Tourette’s may be diagnosed when a person exhibits both multiple motor and one or more vocal tics (although these do not need to be concurrent) over the period of a year, with no more than three consecutive tic-free months. The previous DSM-IV included a requirement for "marked distress or significant impairment in social, occupational or other important areas of functioning", but this requirement was removed in the most recent update of the manual, in recognition that clinicians see patients who meet all the other criteria for Tourette's, but do not have distress or impairment.[40] The onset must have occurred before the age of 18, and cannot be attributed to the "direct physiological effects of a substance or a general medical condition".[6] Hence, other medical conditions that include tics or tic-like movements—such as autism or other causes of tourettism—must be ruled out before conferring a Tourette's diagnosis.
There are no specific medical or screening tests that can be used in diagnosing Tourette's;[20] it is frequently misdiagnosed or underdiagnosed, partly because of the wide expression of severity, ranging from mild (the majority of cases) or moderate, to severe (the rare, but more widely recognized and publicized cases).[25] Coughing, eye blinking and tics that mimic asthma are commonly misdiagnosed.[1]
The diagnosis is made based on observation of the individual's symptoms and family history,[1] and after ruling out secondary causes of tic disorders.[35] In patients with a typical onset and a family history of tics or obsessive–compulsive disorder, a basic physical and neurological examination may be sufficient.[11]
There is no requirement that other comorbid conditions (such as ADHD or OCD) be present,[1] but if a physician believes that there may be another condition present that could explain tics, tests may be ordered as necessary to rule out that condition. An example of this is when diagnostic confusion between tics and seizure activity exists, which would call for an EEG, or if there are symptoms that indicate an MRI to rule out brain abnormalities.[41] TSH levels can be measured to rule out hypothyroidism, which can be a cause of tics. Brain imaging studies are not usually warranted.[41] In teenagers and adults presenting with a sudden onset of tics and other behavioral symptoms, a urine drug screen for cocaine and stimulants might be necessary. If a family history of liver disease is present, serum copper and ceruloplasmin levels can rule out Wilson's disease.[11] Most cases are diagnosed by merely observing a history of tics.[24]
Secondary causes of tics (not related to inherited Tourette syndrome) are commonly referred to as tourettism.[33] Dystonias, choreas, other genetic conditions, and secondary causes of tics should be ruled out in the differential diagnosis for Tourette syndrome.[11] Other conditions that may manifest tics or stereotyped movements include developmental disorders, autism spectrum disorders,[42] and stereotypic movement disorder;[43][44] Sydenham's chorea; idiopathic dystonia; and genetic conditions such as Huntington's disease, neuroacanthocytosis, Hallervorden-Spatz syndrome, Duchenne muscular dystrophy, Wilson's disease, and tuberous sclerosis. Other possibilities include chromosomal disorders such as Down syndrome, Klinefelter syndrome, XYY syndrome and fragile X syndrome. Acquired causes of tics include drug-induced tics, head trauma, encephalitis, stroke, and carbon monoxide poisoning.[11][33] The symptoms of Lesch-Nyhan syndrome may also be confused with Tourette syndrome.[26] Most of these conditions are rarer than tic disorders, and a thorough history and examination may be enough to rule them out, without medical or screening tests.[24]
Screening
Although not all people with Tourette's have comorbid conditions, most Tourette's patients presenting for clinical care at specialty referral centers may exhibit symptoms of other conditions along with their motor and phonic tics.[29] Associated conditions include attention-deficit hyperactivity disorder (ADD or ADHD), obsessive–compulsive disorder (OCD), learning disabilities and sleep disorders.[1] Disruptive behaviors, impaired functioning, or cognitive impairment in patients with comorbid Tourette's and ADHD may be accounted for by the comorbid ADHD, highlighting the importance of identifying and treating comorbid conditions.[1][4][20][27] Disruption from tics is commonly overshadowed by comorbid conditions that present greater interference to the child.[24] Tic disorders in the absence of ADHD do not appear to be associated with disruptive behavior or functional impairment,[45] while impairment in school, family, or peer relations is greater in patients who have more comorbid conditions and often determines whether therapy is needed.[13]
Because comorbid conditions such as OCD and ADHD can be more impairing than tics, these conditions are included in an evaluation of patients presenting with tics. "It is critical to note that the comorbid conditions may determine functional status more strongly than the tic disorder," according to Samuel Zinner, MD.[24] The initial assessment of a patient referred for a tic disorder should include a thorough evaluation, including a family history of tics, ADHD, obsessive–compulsive symptoms, and other chronic medical, psychiatric and neurological conditions. Children and adolescents with TS who have learning difficulties are candidates for psychoeducational testing, particularly if the child also has ADHD.[41] Undiagnosed comorbid conditions may result in functional impairment, and it is necessary to identify and treat these conditions to improve functioning. Complications may include depression, sleep problems, social discomfort and self-injury.[11]
ManagementMain article: Treatment of Tourette syndrome

Clonidine (or the clonidine patch) is one of the medications typically tried first when medication is needed for Tourette's.


The treatment of Tourette's focuses on identifying and helping the individual manage the most troubling or impairing symptoms.[1] Most cases of Tourette's are mild, and do not require pharmacological treatment;[35] instead, psychobehavioral therapy, education, and reassurance may be sufficient.[46] Treatments, where warranted, can be divided into those that target tics and comorbid conditions, which, when present, are often a larger source of impairment than the tics themselves.[41] Not all people with tics have comorbid conditions,[29] but when those conditions are present, they often take treatment priority.
There is no cure for Tourette's and no medication that works universally for all individuals without significant adverse effects. Knowledge, education and understanding are uppermost in management plans for tic disorders.[1] The management of the symptoms of Tourette's may include pharmacological, behavioral and psychological therapies. While pharmacological intervention is reserved for more severe symptoms, other treatments (such as supportive psychotherapy or cognitive behavioral therapy) may help to avoid or ameliorate depression and social isolation, and to improve family support. Educating a patient, family, and surrounding community (such as friends, school, and church) is a key treatment strategy, and may be all that is required in mild cases.[1][47]

Model of a haloperidol molecule. Haloperidol is an antipsychotic medication sometimes used to treat severe cases of Tourette's.


Medication is available to help when symptoms interfere with functioning.[35] The classes of medication with the most proven efficacy in treating tics—typical and atypical neuroleptics including risperidone (trade name[48] Risperdal), ziprasidone (Geodon), haloperidol (Haldol), pimozide (Orap) and fluphenazine (Prolixin)—can have long-term and short-term adverse effects.[41] The antihypertensive agents clonidine (trade name Catapres) and guanfacine (Tenex) are also used to treat tics; studies show variable efficacy, but a lower side effect profile than the neuroleptics.[49] Stimulants and other medications may be useful in treating ADHD when it co-occurs with tic disorders. Drugs from several other classes of medications can be used when stimulant trials fail, including guanfacine (trade name Tenex), atomoxetine (Strattera) and tricyclic antidepressants. Clomipramine (Anafranil), a tricyclic, and SSRIs—a class of antidepressants including fluoxetine (Prozac), sertraline (Zoloft), and fluvoxamine (Luvox)—may be prescribed when a Tourette's patient also has symptoms of obsessive–compulsive disorder. Several other medications have been tried, but evidence to support their use is unconvincing.[41]
Because children with tics often present to physicians when their tics are most severe, and because of the waxing and waning nature of tics, it is recommended that medication not be started immediately or changed often.[24] Frequently, the tics subside with explanation, reassurance, understanding of the condition and a supportive environment.[24] When medication is used, the goal is not to eliminate symptoms: it should be used at the lowest possible dose that manages symptoms without adverse effects, given that these may be more disturbing than the symptoms for which they were prescribed.[24]
Cognitive behavioral therapy (CBT) is a useful treatment when OCD is present,[50] and there is increasing evidence supporting the use of habit reversal in the treatment of tics.[51] Relaxation techniques, such as exercise, yoga or meditation, may be useful in relieving the stress that may aggravate tics, but the majority of behavioral interventions (such as relaxation training and biofeedback, with the exception of habit reversal) have not been systematically evaluated and are not empirically supported therapies for Tourette's.[52]
Prognosis
André Malraux (1901–1976) was a French author, adventurer and Minister of Culture who had Tourette syndrome.[53][54][55][56] President Kennedy, Marie-Madeleine Lioux, Malraux, Jackie Kennedy and Vice President Johnson were photographed at the unveiling of the Mona Lisa at the National Gallery of Art, Washington, DC, in 1963.[57]


Tourette syndrome is a spectrum disorder—its severity ranges over a spectrum from mild to severe. The majority of cases are mild and require no treatment.[35] In these cases, the impact of symptoms on the individual may be mild, to the extent that casual observers might not know of their condition. The overall prognosis is positive, but a minority of children with Tourette syndrome have severe symptoms that persist into adulthood.[30] A study of 46 subjects at 19 years of age found that the symptoms of 80% had minimum to mild impact on their overall functioning, and that the other 20% experienced at least a moderate impact on their overall functioning.[5] The rare minority of severe cases can inhibit or prevent individuals from holding a job or having a fulfilling social life. In a follow-up study of thirty-one adults with Tourette's, all patients completed high school, 52% finished at least two years of college, and 71% were full-time employed or were pursuing higher education.[58]
Regardless of symptom severity, individuals with Tourette's have a normal life span. Although the symptoms may be lifelong and chronic for some, the condition is not degenerative or life-threatening. Intelligence is normal in those with Tourette's, although there may be learning disabilities.[1] Severity of tics early in life does not predict tic severity in later life,[1] and prognosis is generally favorable,[59] although there is no reliable means of predicting the outcome for a particular individual. The gene or genes associated with Tourette's have not been identified, and there is no potential "cure".[59] A higher rate of migraines than the general population and sleep disturbances are reported.[59]
Several studies have demonstrated that the condition in most children improves with maturity. Tics may be at their highest severity at the time that they are diagnosed, and often improve with understanding of the condition by individuals and their families and friends. The statistical age of highest tic severity is typically between eight and twelve, with most individuals experiencing steadily declining tic severity as they pass through adolescence. One study showed no correlation with tic severity and the onset of puberty, in contrast with the popular belief that tics increase at puberty. In many cases, a complete remission of tic symptoms occurs after adolescence.[25][60] However, a study using videotape to record tics in adults found that, although tics diminished in comparison with childhood, and all measures of tic severity improved by adulthood, 90% of adults still had tics. Half of the adults who considered themselves tic-free still displayed evidence of tics.[58]

Tim Howard, goalkeeper for Everton F.C., says, "Tourette's syndrome is not a problem. ... It doesn't affect me one way or another on or off the field."[61]


It is not uncommon for the parents of affected children to be unaware that they, too, may have had tics as children. Because Tourette's tends to subside with maturity, and because milder cases of Tourette's are now more likely to be recognized, the first realization that a parent had tics as a child may not come until their offspring is diagnosed. It is not uncommon for several members of a family to be diagnosed together, as parents bringing children to a physician for an evaluation of tics become aware that they, too, had tics as a child.
Children with Tourette's may suffer socially if their tics are viewed as "bizarre". If a child has disabling tics, or tics that interfere with social or academic functioning, supportive psychotherapy or school accommodations can be helpful.[35] Because comorbid conditions (such as ADHD or OCD) can cause greater impact on overall functioning than tics, a thorough evaluation for comorbidity is called for when symptoms and impairment warrant.[11]
A supportive environment and family generally gives those with Tourette's the skills to manage the disorder.[62][63] People with Tourette's may learn to camouflage socially inappropriate tics or to channel the energy of their tics into a functional endeavor. Accomplished musicians, athletes, public speakers, and professionals from all walks of life are found among people with Tourette's. Outcomes in adulthood are associated more with the perceived significance of having severe tics as a child than with the actual severity of the tics. A person who was misunderstood, punished, or teased at home or at school will fare worse than children who enjoyed an understanding and supportive environment.[5]
Epidemiology
The tics of Tourette syndrome begin in childhood and tend to remit or subside with maturity; thus, a diagnosis may no longer be warranted for many adults, and observed prevalence rates are higher among children than adults.[25] As children pass through adolescence, about one-quarter become tic-free, almost one-half see their tics diminish to a minimal or mild level, and less than one-quarter have persistent tics. Only 5 to 14% of adults experience worse tics in adulthood than in childhood.[1][4]
Tourette syndrome is found among all social, racial and ethnic groups and has been reported in all parts of the world;[1][20] it is three to four times more frequent among males than among females.[2] The reported prevalence of TS varies "according to the source, age, and sex of the sample; the ascertainment procedures; and diagnostic system"[20] from a low of .05% in a 1993 study to a high of 2.9% in a 1998 study.[1]
Up to 1% of the overall population experiences tic disorders, including chronic tics and transient tics of childhood.[45] Chronic tics affect 5% of children, and transient tics affect up to 20%.[64] Robertson (2011) suggests that the prevalence of Tourette syndrome alone in the general population is also 1%, with a range reported between .4% and 3.8% for children ages 5 to 18.[2] Singer (2011) states the prevalence of TS in the overall population at any time is .1% for impairing cases and .6% for all cases,[1] while Bloch et al. (2011) state the overall prevalence as between .3 and 1%.[31] According to Lombroso and Scahill (2008), the emerging consensus is that .1 to 1% of children have Tourette's,[65] with several studies supporting a tighter range of .6 to .8%.[45] Bloch and Leckman (2009) and Swain (2007) report a range of prevalence in children of .4 to .6%,[20][64] while Du et al. (2010) report that 1 to 3% of Western school-age children have Tourette's.[4] Prevalence rates in special education populations are higher.[2] Using year 2000 census data, a prevalence range of .1 to 1% yields an estimate of 53,000–530,000 school-age children with Tourette's in the US,[45] and a prevalence estimate of .1% means that in 2001 about 553,000 people in the UK age 5 or older would have Tourette's. Most cases would be mild and almost unrecognizable in older individuals.[66]
Tourette syndrome was once thought to be rare: in 1972, the US National Institutes of Health (NIH) believed there were fewer than 100 cases in the United States,[67] and a 1973 registry reported only 485 cases worldwide.[68] However, multiple studies published since 2000 have consistently demonstrated that the prevalence is much higher than previously thought.[69] Discrepancies across current and prior prevalence estimates come from several factors: ascertainment bias in earlier samples drawn from clinically referred cases, assessment methods that may fail to detect milder cases, and differences in diagnostic criteria and thresholds.[69] There were few broad-based community studies published before 2000 and until the 1980s, most epidemiological studies of Tourette syndrome were based on individuals referred to tertiary care or specialty clinics.[70] Children with milder symptoms are unlikely to be referred to specialty clinics, so these studies have an inherent bias towards more severe cases.[71] Studies of Tourette syndrome are vulnerable to error because tics vary in intensity and expression, are often intermittent, and are not always recognized by clinicians, patients, family members, friends or teachers;[24][72] approximately 20% of persons with Tourette syndrome do not recognize that they have tics.[24] Newer studies—recognizing that tics may often be undiagnosed and hard to detect—use direct classroom observation and multiple informants (parent, teacher, and trained observers), and therefore record more cases than older studies relying on referrals.[47][73] As the diagnostic threshold and assessment methodology have moved towards recognition of milder cases, the result is an increase in estimated prevalence.[69]
Tourette's is associated with several comorbid conditions, or co-occurring diagnoses, which are often the major source of impairment for an affected child.[20][31] Most individuals with tics do not seek medical attention, so epidemiological studies of TS "reflect a strong ascertainment bias",[31] but among those who do warrant medical attention, the majority have other conditions, and up to 50% have ADHD or OCD.[31] One author reports that a ten-year overview of patient records revealed about 40% of patients with Tourette's have "TS-only" or "pure TS", referring to Tourette syndrome in the absence of ADHD, OCD and other disorders.[28][29] In children with tics, the additional presence of ADHD is associated with functional impairment, disruptive behavior, and tic severity. Other comorbid conditions include self-injurious behaviors (SIB), anxiety, depression, personality disorders, oppositional defiant disorder, and conduct disorders.[74]
History and research directionsMain article: History of Tourette syndrome

Jean-Martin Charcot (1825–1893) was a French neurologist and professor who bestowed the eponym for Tourette syndrome on behalf of his resident, Georges Albert Édouard Brutus Gilles de la Tourette. Charcot is shown here during a lesson with a "hysterical" woman patient at the Salpêtrière hospital.


The first presentation of Tourette syndrome is thought to be in a 1489 book, Malleus maleficarum ("Witch's hammer") by Jakob Sprenger and Heinrich Kraemer, describing a priest whose tics were "believed to be related to possession by the devil".[75] A French doctor, Jean Marc Gaspard Itard, reported the first case of Tourette syndrome in 1825,[76] describing Marquise de Dampierre, an important woman of nobility in her time.[77] Jean-Martin Charcot, an influential French physician, assigned his resident Georges Albert Édouard Brutus Gilles de la Tourette, a French physician and neurologist, to study patients at the Salpêtrière Hospital, with the goal of defining an illness distinct from hysteria and from chorea.[23]
In 1885, Gilles de la Tourette published an account in Study of a Nervous Affliction describing nine persons with "convulsive tic disorder", concluding that a new clinical category should be defined.[78][79] The eponym was later bestowed by Charcot after and on behalf of Gilles de la Tourette.[23][80]
Little progress was made over the next century in explaining or treating tics, and a psychogenic view prevailed well into the 20th century.[23] The possibility that movement disorders, including Tourette syndrome, might have an organic origin was raised when an encephalitis epidemic from 1918–1926 led to a subsequent epidemic of tic disorders.[81]
During the 1960s and 1970s, as the beneficial effects of haloperidol (Haldol) on tics became known, the psychoanalytic approach to Tourette syndrome was questioned.[82] The turning point came in 1965, when Arthur K. Shapiro—described as "the father of modern tic disorder research"[83]—treated a Tourette’s patient with haloperidol, and published a paper criticizing the psychoanalytic approach.[81]
Since the 1990s, a more neutral view of Tourette's has emerged, in which biological vulnerability and adverse environmental events are seen to interact.[23][24] In 2000, the American Psychiatric Association published the DSM-IV-TR, revising the text of DSM-IV to no longer require that symptoms of tic disorders cause distress or impair functioning.[84]
Findings since 1999 have advanced TS science in the areas of genetics, neuroimaging, neurophysiology, and neuropathology. Questions remain regarding how best to classify Tourette syndrome, and how closely Tourette's is related to other movement disorders or psychiatric disorders. Good epidemiologic data is still lacking, and available treatments are not risk free and not always well tolerated.[85] High-profile media coverage focuses on treatments that do not have established safety or efficacy, such as deep brain stimulation, and alternative therapies involving unstudied efficacy and side effects are pursued by many parents.[37]
Society and cultureMain article: Sociological and cultural aspects of Tourette syndrome

Samuel Johnson (1709–1784) circa 1772. Johnson likely had Tourette syndrome.


Not everyone with Tourette's wants treatment or a "cure", especially if that means they may "lose" something else in the process.[86][87] Researchers Leckman and Cohen, and former Tourette Syndrome Association national board member Kathryn Taubert, believe that there may be latent advantages associated with an individual's genetic vulnerability to developing Tourette syndrome, such as a heightened awareness and increased attention to detail and surroundings that may have adaptive value.[88] There is evidence to support the clinical lore that children with "TS-only" (Tourette's in the absence of comorbid conditions) are unusually gifted: neuropsychological studies have identified advantages in children with TS-only.[29][89] One study found that children with TS-only are faster than the average for their age group on timed tests of motor coordination.[90]
Notable individuals with Tourette syndrome are found in all walks of life, including musicians, athletes, media figures, teachers, physicians and authors.[91] The best-known example of a person who may have used obsessive–compulsive traits to advantage is Samuel Johnson, the 18th-century English man of letters, who likely had Tourette syndrome as evidenced by the writings of James Boswell.[92][93] Johnson wrote A Dictionary of the English Language in 1747, and was a prolific writer, poet, and critic.
Although it has been speculated that Mozart had Tourette's,[94][95] no Tourette's expert or organization has presented credible evidence to support such a conclusion,[95] and there are problems with the arguments supporting the diagnosis: tics are not transferred to the written form, as is supposed with Mozart's scatological writings; the medical history in retrospect is not thorough; side effects due to other conditions may be misinterpreted; "it is not proven whether written documents can account for the existence of a vocal tic" and "the evidence of motor tics in Mozart's life is doubtful".[96]
The entertainment industry has been criticized for depicting those with Tourette syndrome as social misfits whose only tic is coprolalia, which has furthered stigmatization and the public's misunderstanding of those with Tourette's.[97] The coprolalic symptoms of Tourette's are also fodder for radio and television talk shows in the US[98] and in the British media.[99]


 楼主| 发表于 2013-7-25 21:43:17 | 显示全部楼层
图雷特氏综合症英语Tourette Syndrome,又称抽动症)是一种抽动综合症
1885年,图雷特氏综合症首先被法国医生Gilles de la Tourette发现并描述,是一种非常严重的抽动性疾病,包括运动抽动、声音抽动以及综合抽动。诊断标准包括:在18岁以前发病,有不断复发、无法由意志控制、快速且盲目的影响大部分肌肉群的动作痉挛或多种声音痉挛。在一个阶段内,可能的严重程度可以有变化,而症状会持续一年以上。
值得注意的是,该诊断标准是相对于个人,并不是绝对的。很少有图雷特氏综合症的发病在21岁后,且“无法由意志控制”的标准很难定义。实际上,有些病人会有一种内部意志驱使运动的感觉,并伴随着心理紧张以及焦虑。该诊断标准里,并没有提及图雷特氏综合症病人经常会表现出来的其他缺陷,例如:注意力问题、强迫症以及ADHD问题。
  • 2008年美国电影《叫我第一名》(Front of the Class),即讲述了一名图雷特氏综合症患者通过自强不息的努力,成为一名优秀教师的真实故事。
  • 2010年德国电影 Vincent will Meer 也讲述图雷特氏综合症。
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