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可能为一种新的常染色体隐性综合征,表现为胼胝体部分发育不全、脑桥发育不全、局灶性白质改变、肌张力减退、智力发育迟缓及轻微异常。

Possible new autosomal recessive syndrome of partial agenesis of the corpus callosum, pontine hypoplasia, focal white matter changes, hypotonia, mental retardation, and minor anomalies.

作者信息

Jonas R E, Kimonis V E, Morales A

机构信息

Department of Pediatrics, Southern Illinois University School of Medicine, Springfield 62794-9230, USA.

出版信息

Am J Med Genet. 1997 Dec 12;73(2):184-8.

PMID:9409870
Abstract

We describe a brother and sister with severe developmental delay, hypotonia, partial agenesis of the corpus callosum, pontine hypoplasia, focal white matter degenerative abnormalities, macrocrania, frontal bossing, deep-set eyes, and hypertelorism. The brother also had Duane syndrome type II and an ectopic right ureter. The coexistence of these multiple physical and brain abnormalities in a brother and sister suggests a new autosomal recessive syndrome with a slowly progressive course.

摘要

我们描述了一对患有严重发育迟缓、肌张力减退、胼胝体部分发育不全、脑桥发育不全、局灶性白质退行性异常、巨头症、额部隆起、眼窝深陷和眼距过宽的兄妹。哥哥还患有II型杜安综合征和右侧异位输尿管。兄妹中这些多种身体和脑部异常的共存提示一种新的常染色体隐性综合征,病程呈缓慢进展。

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