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晚发性婴儿常染色体隐性遗传性肌强直、智力发育迟缓及骨骼异常:一种新的常染色体隐性综合征。

Late infantile autosomal recessive myotonia, mental retardation, and skeletal abnormalities: a new autosomal recessive syndrome.

作者信息

Richieri-Costa A, Garcia da Silva S M, Frota-Pessoa O

出版信息

J Med Genet. 1984 Apr;21(2):103-7. doi: 10.1136/jmg.21.2.103.

Abstract

Four sibs of non-consanguineous parents who had myotonia from late infancy are described. Mild to moderate mental retardation, severe bone abnormalities of the vertebral column (mainly in the thoracolumbar region), and short stature were also observed. Autosomal recessive inheritance is demonstrated. These cases are compared with reported cases of the Schwartz-Jampel syndrome.

摘要

本文描述了4名非近亲父母的同胞兄弟姐妹,他们自婴儿期晚期起就患有肌强直。还观察到轻度至中度智力发育迟缓、严重的脊柱骨骼异常(主要在胸腰段)和身材矮小。证实为常染色体隐性遗传。将这些病例与已报道的施瓦茨 - 詹佩尔综合征病例进行了比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a2b/1049235/9e30f9e09dbd/jmedgene00100-0024-a.jpg

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