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[一种X连锁隐性肩胛背型肌营养不良症家族]

[A family of scapula-back type of x-linked recessive muscular dystrophy].

作者信息

Ji X W

出版信息

Zhonghua Shen Jing Jing Shen Ke Za Zhi. 1989 Jun;22(3):136-8, 190.

PMID:2591265
Abstract

In this paper are described seven men with a scapula-back type of x-linked recessive muscular dystrophy in a family. Onset began in boyhood. The scapula-back muscles were affected, but the calf muscles were normal. All of the patients were able to walk. The oldest patient was thirty-seven years old. Muscular dystrophy was confirmed by electro-myography (EMG), pathologic and CPK examinations. Pedigree analysis indicated x-linked recessive inheritance.

摘要

本文描述了一个家族中七名患有X连锁隐性肩胛背型肌营养不良症的男性。发病始于童年。肩胛背肌受累,但小腿肌肉正常。所有患者都能行走。年龄最大的患者37岁。通过肌电图(EMG)、病理检查和肌酸磷酸激酶(CPK)检查确诊为肌营养不良症。系谱分析表明为X连锁隐性遗传。

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