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自闭症、智力迟钝和染色体异常。

Autism, mental retardation, and chromosomal abnormalities.

作者信息

Mariner R, Jackson A W, Levitas A, Hagerman R J, Braden M, McBogg P M, Smith A C, Berry R

出版信息

J Autism Dev Disord. 1986 Dec;16(4):425-40. doi: 10.1007/BF01531709.

Abstract

There are reports of sex chromosomal abnormalities including XXY, XYY, and fragile X karyotypes in autistic individuals, but structural autosomal defects have rarely been reported. This paper presents four patients with autism, mental retardation, minor dysmorphic features, and structural autosomal defects. These patients shared autistic features including fascination with inanimate objects, catastrophic reactions to changes in their environment or their daily routine, echolalia, and poor relatedness; IQ scores indicate mild to severe retardation. Their autosomal abnormalities included inversion/duplications of 3p and 16q, 5p+, and 17p-. Parental chromosomes were all normal. Chromosomal analysis should be performed on mentally retarded, autistic individuals, especially those with minor physical anomalies and no specific etiology for their retardation.

摘要

有报告称自闭症个体存在性染色体异常,包括XXY、XYY和脆性X核型,但常染色体结构缺陷鲜有报道。本文介绍了四名患有自闭症、智力迟钝、轻微畸形特征和常染色体结构缺陷的患者。这些患者具有共同的自闭症特征,包括对无生命物体着迷、对环境或日常生活变化产生灾难性反应、模仿言语以及社交关系差;智商测试结果表明存在轻度至重度智力迟钝。他们的常染色体异常包括3号染色体短臂和16号染色体长臂的倒位/重复、5号染色体短臂增加以及17号染色体短臂缺失。父母的染色体均正常。对于智力迟钝的自闭症个体,尤其是那些有轻微身体异常且智力迟钝无特定病因的个体,应进行染色体分析。

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