Heterogeneity of nemaline myopathy. A follow-up study of 13 cases.

Pediatric neuroscience Pub Date : 1988-01-01
E Shahar, R C Tervo, E G Murphy
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引用次数: 0

Abstract

The marked heterogeneity of nemaline myopathy is again shown in the present series of 13 patients. Most children have a long-standing, mild, and slowly progressing proximal myopathy. Two brothers with extreme weakness died during the neonatal period of respiratory failure representing the X-linked variant. One adult with proximal weakness was also diagnosed as having nemaline myopathy. An unusual course was observed in 2 infants who initially had moderate weakness but subsequently developed severe generalized weakness including respiratory muscles. This led to irreversible respiratory failure requiring continuous ventilatory support for as long as 9 and 15 years, respectively. Although uncommon, the possibility of an imminent respiratory failure in initially weak infants should also be taken into account within the clinical spectrum of nemaline myopathy.

线状肌病的异质性。对13例病例进行随访研究。
在本系列的13例患者中再次显示出线状肌病的显著异质性。大多数儿童有一个长期的,轻度的,进展缓慢的近端肌病。两个极度虚弱的兄弟在新生儿时期死于呼吸衰竭,代表x连锁变异。一个成年人与近端无力也被诊断为有线状肌病。在2例婴儿中观察到一个不寻常的过程,他们最初有中度虚弱,但随后发展为包括呼吸肌在内的严重全身性虚弱。这导致不可逆转的呼吸衰竭,分别需要长达9年和15年的持续通气支持。虽然不常见,但在最初虚弱的婴儿中,迫在眉睫的呼吸衰竭的可能性也应考虑到线状肌病的临床谱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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