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弥漫性瓦解障碍:雷特综合征和婴儿痴呆(海勒综合征)是其亚型吗?

Pervasive disintegrative disorder: are Rett syndrome and Heller dementia infantilis subtypes?

作者信息

Burd L, Fisher W, Kerbeshian J

机构信息

Child Evaluation and Treatment Program, Medical Center Rehabilitation Hospital, Grand Forks, North Dakota 58202.

出版信息

Dev Med Child Neurol. 1989 Oct;31(5):609-16. doi: 10.1111/j.1469-8749.1989.tb04046.x.

Abstract

Children with developmental regression and emerging symptoms of autism have been given a variety of classifications. The authors compare two boys with Heller dementia with six girls with Rett syndrome. They all differed from children with classic autism in that they had normal prenatal and perinatal periods, followed by marked developmental regression, after which they acquired few or no skills. The boys differed from the girls in terms of estimated prevalence, age at onset, stereotypic breathing patterns, midline hand stereotypies, hand and gait apraxia and speech development. It is suggested that these children should be distinguished from those with classic autism, and should be classified as 'pervasive disintegrative disorder, Heller type' and 'pervasive disintegrative disorder, Rett type'.

摘要

患有发育倒退和新出现自闭症症状的儿童被给予了多种分类。作者将两名患有海勒氏痴呆症的男孩与六名患有雷特综合征的女孩进行了比较。他们都与典型自闭症儿童不同,因为他们在产前和围产期正常,随后出现明显的发育倒退,之后几乎没有获得技能。男孩在估计患病率、发病年龄、刻板呼吸模式、中线手部刻板动作、手部和步态失用症以及语言发展方面与女孩不同。建议将这些儿童与典型自闭症儿童区分开来,并应分类为“弥漫性发育障碍,海勒型”和“弥漫性发育障碍,雷特型”。

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