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博耶森-福斯曼-莱曼综合征。一项家族研究。

The Borjeson-Forssman-Lehmann syndrome. A family study.

作者信息

Dereymaeker A M, Fryns J P, Hoefnagels M, Heremans G, Marien J, van den Berghe H

出版信息

Clin Genet. 1986 Apr;29(4):317-20.

PMID:3720009
Abstract

The propositus of this report presents a peculiar dysmorphic syndrome associated with severe mental retardation and epileptic attacks. Morphological stigmata include a round, fatty face with large, somewhat protruding tongue, large normally formed ears, relative microcephaly, abundant abdominal fat, dwarfism with hyperkyphosis and short neck. Analogous phenotypic abnormalities were present in the mother and a maternal cousin. The clinical and familial findings in this apparently rare mental retardation syndrome with apparently X-linked dominant or autosomal dominant inheritance with variable expression and penetrance are discussed.

摘要

本报告的先证者表现出一种特殊的畸形综合征,伴有严重智力迟钝和癫痫发作。形态学特征包括圆形的胖脸、大且稍突出的舌头、正常形态的大耳朵、相对小头畸形、腹部脂肪丰富、伴有脊柱后凸的侏儒症和短颈。母亲和一位母系表亲也存在类似的表型异常。本文讨论了这种明显罕见的智力迟钝综合征的临床和家族性发现,其遗传方式明显为X连锁显性或常染色体显性遗传,具有可变的表达和外显率。

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