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脊髓性肌萎缩症所致膈肌麻痹。婴儿呼吸衰竭的一个未被认识的病因?

Diaphragmatic paralysis due to spinal muscular atrophy. An unrecognised cause of respiratory failure in infancy?

作者信息

McWilliam R C, Gardner-Medwin D, Doyle D, Stephenson J B

出版信息

Arch Dis Child. 1985 Feb;60(2):145-9. doi: 10.1136/adc.60.2.145.

Abstract

An unusual form of spinal muscular atrophy presenting with respiratory failure was observed in four infants from two families. In one, whose death was attributed to pneumonia, the diagnosis was inferred retrospectively after two siblings died from an identical illness and were shown to have diaphragmatic paralysis and the typical electrophysiological and histological features of spinal muscular atrophy. Other signs of skeletal muscular weakness were absent or inconspicuous. The fourth, unrelated infant presented in an identical way but has survived for over a year on a ventilator. Two months after the onset of respiratory paralysis, more extensive skeletal muscular weakness was seen. Other infants, dying of unexplained respiratory illness, may have this disorder and some may be included in the miscellany of disorders that constitute the sudden infant death syndrome.

摘要

在来自两个家庭的四名婴儿中观察到一种以呼吸衰竭为表现的不寻常形式的脊髓性肌萎缩。其中一个家庭中,一名婴儿死于肺炎,在另外两名患有相同疾病并被证明有膈肌麻痹以及脊髓性肌萎缩典型电生理和组织学特征的兄弟姐妹死亡后,该病例被追溯诊断。未发现或仅有不明显的骨骼肌无力的其他体征。第四名与之无关的婴儿也以同样的方式发病,但依靠呼吸机存活了一年多。呼吸麻痹发作两个月后,出现了更广泛的骨骼肌无力。其他死于不明原因呼吸道疾病的婴儿可能患有这种疾病,其中一些可能被归入构成婴儿猝死综合征的各种疾病之中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9e5/1777133/ee681f6a7036/archdisch00725-0064-a.jpg

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