ul Hassan Z, Fastabend C P, Mohanty P K, Isaacs E R
Circulation. 1979 Dec;60(6):1365-9. doi: 10.1161/01.cir.60.6.1365.
This report describes a family showing muscular dystrophy and atrioventricular block with an x-linked hereditary transmission. Among a known pedigree of 101 family members, 12 males were found to have skeletal muscle involvement and six needed pacemakers around age 30 years. Unlike the x-linked muscular dystrophies of Duchenne and of Becker, the predominant skeletal involvement was in humeral muscles, was usually very mild, and did not produce incapacitation. Cardiac involvement consisted of various atrial arrhythmias and atrioventricular block. The few sporadic reports of other families that describe the same disease under different names are briefly reviewed. Recognition of this subtle muscular dystrophy is important for early detection of incipient complete atrioventricular block to prevent fatal complications by pacemaker insertion.
本报告描述了一个表现为肌肉萎缩症和房室传导阻滞且呈X连锁遗传的家族。在一个已知的由101名家庭成员组成的谱系中,发现12名男性有骨骼肌受累情况,其中6人在30岁左右需要安装起搏器。与杜兴氏和贝克氏X连锁肌肉萎缩症不同,主要的骨骼肌受累部位是肱部肌肉,通常非常轻微,不会导致失能。心脏受累表现为各种房性心律失常和房室传导阻滞。本文简要回顾了其他一些家族以不同名称描述同一疾病的少数散发病例报告。认识到这种隐匿性肌肉萎缩症对于早期发现初期完全性房室传导阻滞以通过植入起搏器预防致命并发症很重要。