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首页> 外文期刊>Neurology: Official Journal of the American Academy of Neurology >Influence of family history on clinical expression of Tourette's syndrome.
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Influence of family history on clinical expression of Tourette's syndrome.

机译:家族史对临床表现的影响妥瑞氏综合征。

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OBJECTIVE: To determine the influence of family history on clinical expression of Tourette's syndrome (TS). BACKGROUND: Recent studies have suggested that clinical expression of TS is similar among sporadic (SP) and familial patients but may be influenced by bilineal (BIL) transmission of tics or obsessive-compulsive behavior (OCB) in high-density pedigrees. METHODS: The authors used family history methodology, supported by direct examination of affected relatives in 73 of familial patients, to determine the frequency of SP TS, and of unilineal (UNL) and BIL transmission of tics or OCB in 111 consecutively ascertained juvenile TS patients. For individuals in each group, severity of tics, attention deficit hyperactivity disorder (ADHD), and OCB were assessed at presentation and after a mean follow-up interval of 2.6 years, using the Tourette's Syndrome Global Scale and the Clinical Global Impression scales. The phenomenology of OCB was evaluated using the symptom checklist of the Children's Yale-Brown Obsessive Compulsive Scale. RESULTS: The authors documented BIL transmission of tics in seven patients (6). Patient age and sex were similar for the SP (n = 21; 19), UNL (n = 66; 59), and BIL (n = 24; 22) groups, as was ADHD and tic severity at presentation and follow-up. Severity of OCB differed significantly between groups, with moderate to severe OCB affecting 5 of SP, 12 of UNL, and 37 of BIL patients at presentation (p = 0.007), and 5 of SP, 17 of UNL, and 54 of BIL patients at follow-up (p = 0.0001). Relative to UNL or SP patients, BIL patients were more likely to exhibit self-injurious behaviors (p = 0.0005). CONCLUSIONS: OCB is less prominent in SP than in familial TS, perhaps reflecting a more restricted pathophysiology in this subgroup. Although BIL transmission of tics is relatively infrequent in consecutive TS pedigrees, cotransmission of OCB from an otherwise unaffected parent is common and significantly influences development of OCB and self-injurious behaviors, but not tics, in offspring. Genetic heterogeneity, epigenetic factors, and gene-environment interactions may play a more important role than genetic dosage effects in determining tic severity in TS.
机译:目的:确定家庭的影响历史上的图雷特综合症的临床表现综合征(TS)。建议TS的临床表现类似的零星(SP)和家族性患者但是可能受到bilineal (BIL)抽搐或强迫性的传播高密度族谱行为(时常)。方法:作者使用家族史支持的方法,直接检查影响亲属在73%的家族性患者,确定的频率SP TS,unilineal(多人)和比尔抽搐或传播时常在111年连续确定青少年TS病人。抽搐,注意缺陷多动障碍(ADHD),时常在演示和评估在平均2.6年的随访时间间隔之后,使用全球规模和妥瑞氏综合征全球临床印象量表。现象学的台籍干部是评估使用症状的儿童Yale-Brown清单强迫性的规模。记录基本脉冲电平传输七的抽搐病人(6%)。SP (n = 21;基本脉冲电平(n = 24;在表示和后续的严重性。的台籍干部群体之间显著不同,有中度到重度的台籍干部影响SP的5%,贵校的12%,和37%的BIL病人演讲(p = 0.007),和5%的SP, 17%的多人,54%的BIL病人在随访(p =0.0001)。患者更有可能显示出有自伤行为(p = 0.0005)。结论:SP的台籍干部不太突出家族TS,也许反映了更多的限制在这组病理生理学。抽搐是相对较少的传播连续TS的起源,cotransmission台籍干部父是普遍的,否则不受影响台籍干部和显著影响发展有自伤行为,但不抽搐的后代。可能因素,基因-环境相互作用比基因剂量扮演更重要的角色在TS效果在决定抽搐严重程度。

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