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重度智力障碍的遗传预后

Genetic prognosis in severe mental handicap.

作者信息

Angeli E, Kirman B

出版信息

J Ment Defic Res. 1975 Sep-Dec;19(3-4):173-93. doi: 10.1111/j.1365-2788.1975.tb01271.x.

Abstract

698 children below age sixteen years with severe mental handicap (below IQ50) who were admitted to hospital between 1956 and 1959 were surveyed for genetic prognosis. They were divided into 23.7% ascribed primarily to environmental factors, 50.9% unclassified aetiologically, 16.2% of Down's syndrome, 5.3% other genetic syndromes and 3.9% with congenital hydrocephalus. The incidence of a similar degree of mental retardation among the sibs of 660 whose families were traced, was 1.1% in the "environmental" group; 4.7% for the unclassified; 1.7% for Down's syndrome, 11.5% for other genetic syndromes and 4.3% for hydrocephalus with spina bifida. There were no affected sibs of the uncomplicated cases of congenital hydrocephalus. This survey underlines the fact that a high proportion of cases of mental handicap remain without aetiological diagnosis. It emphasises the value of such a diagnosis for genetic counselling. Advice given depends on the circumstances of the particular case which requires a detailed social history and sympathetic rapport by members of the team as well as appropriate clinical expertise (Kirman, 1971, 1972). When families with similarly affected new relative or previous severely mentally handicapped sibs are set aside, the recurrent risk for unclassified cases is reduced to three per cent.

摘要

对1956年至1959年间入院的698名16岁以下重度智力障碍(智商低于50)儿童进行了遗传预后调查。这些儿童被分为:主要归因于环境因素的占23.7%,病因未分类的占50.9%,唐氏综合征的占16.2%,其他遗传综合征的占5.3%,先天性脑积水的占3.9%。在追踪到家庭情况的660名儿童的同胞中,类似程度智力迟钝的发生率为:“环境”组1.1%;未分类组4.7%;唐氏综合征组1.7%;其他遗传综合征组11.5%;脊柱裂合并脑积水组4.3%。先天性脑积水单纯病例没有受影响的同胞。这项调查强调了一个事实,即很大一部分智力障碍病例仍未得到病因诊断。它强调了这种诊断对遗传咨询的价值。所提供的建议取决于具体病例的情况,这需要详细的社会史、团队成员的同情态度以及适当的临床专业知识(Kirman,1971年,1972年)。当把有类似受影响新亲属或之前有重度智力障碍同胞的家庭排除在外时,未分类病例的复发风险降至3%。

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