Myopathy and neurogenic muscular atrophy in unexpected cardiopulmonary arrest

被引：2

作者：

Kawashima, Hisashi ^{[1
]}

Ishii, Chiako

Yamanaka, Gaku

Ioi, Hiroaki

Nishimata, Shigeo

Kashiwagi, Yasuyo

Takekuma, Kouji

Miyajima, Tasuku

Hoshika, Akinori

Nishino, Ichizo ^{[2
]}

Nonaka, Ikuya ^{[2
]}

机构：

[1] Tokyo Med Univ, Dept Pediat, Shinjuku Ku, Tokyo 1600023, Japan

[2] Natl Ctr Neurol & Psychiat, Natl Inst Neurosci, Dept Neuromuscular Res, Tokyo, Japan

来源：

PEDIATRICS INTERNATIONAL | 2011年 / 53卷 / 02期

关键词：

cardiopulmonary arrest; congenital fiber type disproportion; nemaline myopathy; spinal muscular atrophy; sudden unexpected death; FATAL NEMALINE MYOPATHY; RESPIRATORY-DISTRESS; INFANCY; DISEASE; FORM;

D O I：

10.1111/j.1442-200X.2010.03211.x

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Background: Neuromuscular disorders can be the cause of sudden death of infants because of their weakness and gastroesophageal reflux (GER). Methods: Muscle biopsy and genetic studies were performed by usual method. Results: In this report four cases of infants with neuromuscular disorders (two cases of congenital myopathy and two cases of spinal muscular atrophy) who had unexpected cardiopulmonary arrest on arrival (CPAOA) are presented. Two of the cases did not show any symptoms, such as muscle weakness prior to CPAOA. The diagnosis was based on the results of the muscle biopsy and genetic examination. Conclusion: These results suggest that sudden infant death caused by neuromuscular disorders should be considered.

引用

页码：159 / 161

页数：3

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