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雷特综合征的自闭症障碍症状。

Autistic disorder symptoms in Rett syndrome.

机构信息

Leiden University, The Netherlands.

出版信息

Autism. 2009 Nov;13(6):567-81. doi: 10.1177/1362361309338184.

Abstract

According to the major classification systems it is not possible to diagnose a comorbid autistic disorder in persons with Rett syndrome. However, this is a controversial issue, and given the level of functioning of persons with Rett syndrome, the autistic disorder is expected to be present in a comparable proportion as in people with the same level of functioning. To investigate, parents of 52 females with classical and atypical Rett syndrome (2.4-49.3 years) completed the Developmental Behavior Checklist (DBC), the Diagnostic Interview for Social and Communication Disorders (DISCO) and the Dutch Vineland Screener 0-6 (VS 0-6). All participants had a severe to profound intellectual disability (ID) according to the VS 0-6. Behavior indicated an autistic disorder in 42 (DBC) to 58 percent (DISCO) of the Rett cases. Autistic behavior had decreased in 19 percent such that they no longer met the criteria for autistic disorder. Some participants were suspected of having a comorbid autistic disorder, though not more often than can be expected at their level of functioning. Clinicians should be aware of the possibility of a comorbid autistic disorder as much as they should be in other people with this level of functioning.

摘要

根据主要分类系统,不可能在雷特综合征患者中诊断出共患自闭症障碍。然而,这是一个有争议的问题,鉴于雷特综合征患者的功能水平,预计自闭症障碍的患病率与具有相同功能水平的人群相当。为了进行调查,52 名经典和非典型雷特综合征女性(2.4-49.3 岁)的父母完成了发育行为检查表(DBC)、社交和沟通障碍诊断访谈(DISCO)和荷兰维宁顿筛查器 0-6(VS 0-6)。所有参与者根据 VS 0-6 均存在严重至极重度智力障碍(ID)。行为表明 42 名(DBC)至 58 名(DISCO)雷特患者存在自闭症障碍。19%的自闭症行为有所减少,以至于他们不再符合自闭症障碍的标准。一些参与者被怀疑患有共患自闭症障碍,但并不比在其功能水平上预期的更多。临床医生应该意识到共患自闭症障碍的可能性,就像他们在具有相同功能水平的其他人中一样。

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