Percy A, Gillberg C, Hagberg B, Witt-Engerström I
Rett Center, Baylor College of Medicine, Houston, Texas.
Neurol Clin. 1990 Aug;8(3):659-76.
Rett syndrome is a disorder noted to date only in females and characterized by a pervasive developmental disability following apparently normal early infancy. In addition to gait difficulties, stereotypic hand movements, and loss of communication and purposeful hand skills, autistic-like behavior is an early sign that often results in misdiagnosis. Despite these significant clinical abnormalities, neuropathologic features are modest, and no consistent laboratory abnormality or diagnostic marker has been identified. The current status of research in RS is considered within the context of autism and other disorders in which autistic features may occur, such as the fragile X syndrome. The concept of autism as neurobiologically based behavior is developed. As such, autism is regarded as an umbrella category containing an ever-expanding list of specific disorders.
雷特综合征是一种迄今为止仅在女性中发现的疾病,其特征是在婴儿早期看似正常之后出现广泛性发育障碍。除了步态困难、刻板的手部动作以及沟通和有目的手部技能丧失外,类似自闭症的行为是一个早期迹象,常常导致误诊。尽管存在这些显著的临床异常,但神经病理学特征并不明显,并且尚未发现一致的实验室异常或诊断标志物。本文在自闭症及其他可能出现自闭症特征的疾病(如脆性X综合征)的背景下,探讨了雷特综合征的研究现状。文中阐述了自闭症作为基于神经生物学的行为这一概念。因此,自闭症被视为一个涵盖范围不断扩大的特定疾病列表的总括类别。