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一种小头畸形、智力迟钝、特殊面容、腭裂和体重不足的综合征。

A syndrome of microcephaly, mental retardation, unusual facies, cleft palate, and weight deficiency.

作者信息

Weaver D D, Williams C P

出版信息

Birth Defects Orig Artic Ser. 1977;13(3B):69-84.

PMID:890101
Abstract

A brother and sister with a distinctive, apparently previously undescribed dysmorphic/mental retardation syndrome are presented. The major features of their condition include moderate-to-severe mental retardation, microcephaly, weight deficiency, prominent ears, midfacial hypoplasia, small mouth, cleft palate, clinodactyly of the fingers, delayed osseous maturation and generalized bone hypoplasia. Of these, the most prominent physical feature is the weight deficiency which is most likely the result of a decrease in muscle, bone, brain and subcutaneous tissue mass. No underlying biochemical defect, chromosome abnormality, environmental agent or infection has been found to explain this condition. An autosomal recessive mode of inheritance is suggested.

摘要

本文报告了一对患有独特的、显然以前未被描述过的畸形/智力发育迟缓综合征的兄妹。他们病情的主要特征包括中度至重度智力发育迟缓、小头畸形、体重不足、耳朵突出、面中部发育不全、小嘴、腭裂、手指尺侧偏斜、骨成熟延迟和全身骨发育不全。其中,最突出的身体特征是体重不足,这很可能是肌肉、骨骼、大脑和皮下组织质量减少的结果。尚未发现潜在的生化缺陷、染色体异常、环境因素或感染来解释这种情况。提示为常染色体隐性遗传模式。

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Familial holoprosencephaly.家族性前脑无裂畸形
Birth Defects Orig Artic Ser. 1971 Jun;7(7):136-42.

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