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胼胝体发育不全、痉挛性四肢瘫以及CT扫描显示侧脑室壁不规则。一种独特的X连锁智力障碍综合征?

Corpus callosum agenesis, spastic quadriparesis and irregular lining of the lateral ventricles on CT-scan. A distinct X-linked mental retardation syndrome?

作者信息

Vles J S, Fryns J P, Folmer K, Boon P, Buttiens M, Grubben C, Janevski B

机构信息

Department of Child Neurology, University of Maastricht, The Netherlands.

出版信息

Genet Couns. 1990;1(2):97-102.

PMID:2081003
Abstract

This report gives a description of 4 male patients, two of whom are sibs, two of whom are uncle and cousin. They appear to have psychomotor retardation, spastic quadriparesis and on CT (partial) agencies of the corpus callosum, and irregular lining of the lateral ventricles, without craniofacial abnormalities or seizures. Although the mode of inheritance of agenesis of the corpus callosum is still difficult to establish, in these 4 male patients an X-linked recessive inheritance is the most likely mode. A review of the literature with concern to the heredity of agenesis of the corpus callosum is presented. The clinical and neurological findings in the present four male patients allow for the delineation of a new X-linked mental retardation syndrome.

摘要

本报告描述了4名男性患者,其中两名是同胞兄弟,两名是叔侄关系。他们表现出精神运动发育迟缓、痉挛性四肢瘫痪,CT显示胼胝体部分发育不全,侧脑室壁不规则,无颅面异常或癫痫发作。尽管胼胝体发育不全的遗传模式仍难以确定,但在这4名男性患者中,X连锁隐性遗传是最可能的模式。本文对胼胝体发育不全的遗传相关文献进行了综述。目前这4名男性患者的临床和神经学表现有助于明确一种新的X连锁智力障碍综合征。

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1
Corpus callosum agenesis, spastic quadriparesis and irregular lining of the lateral ventricles on CT-scan. A distinct X-linked mental retardation syndrome?胼胝体发育不全、痉挛性四肢瘫以及CT扫描显示侧脑室壁不规则。一种独特的X连锁智力障碍综合征?
Genet Couns. 1990;1(2):97-102.
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X-linked mental retardation with agenesis of the corpus callosum.
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Agenesis of the corpus callosum associated with MASA syndrome.胼胝体发育不全与MASA综合征相关。
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Agenesis of the corpus callosum: sonographic features.胼胝体发育不全:超声特征
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Agenesis of the corpus callosum, infantile spasms, spastic quadriplegia, microcephaly and severe mental retardation in three siblings.三例同胞兄弟姐妹患胼胝体发育不全、婴儿痉挛症、痉挛性四肢瘫、小头畸形及严重智力发育迟缓。
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CRASH syndrome: clinical spectrum of corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraparesis and hydrocephalus due to mutations in one single gene, L1.CRASH综合征:由于单个基因L1突变导致的胼胝体发育不全、智力迟钝、拇指内收、痉挛性截瘫和脑积水的临床谱系。
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New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation.伴有独特面部外观和生长发育迟缓的新型X连锁智力障碍(XLMR)综合征。
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X linked recessive inheritance of agenesis of the corpus callosum.胼胝体发育不全的X连锁隐性遗传。
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X-linked spastic paraplegia.X连锁痉挛性截瘫
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