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与发作性呼吸暂停和婴儿猝死相关的先天性肌无力综合征

Congenital myasthenic syndrome associated with episodic apnea and sudden infant death.

作者信息

Byring R F, Pihko H, Tsujino A, Shen X-M, Gustafsson B, Hackman P, Ohno K, Engel A G, Udd B

机构信息

Vaasa Central Hospital, Hietalahdenkatu 2-4, FIN-65130, Vaasa, Finland.

出版信息

Neuromuscul Disord. 2002 Aug;12(6):548-53. doi: 10.1016/s0960-8966(01)00336-4.

Abstract

The sudden infant death syndrome has multiple etiologies. Some congenital myasthenic syndromes can cause sudden infant death syndrome by apnea, but the frequency of this etiology is unknown. We report here a young patient with sudden respiratory crises culminating in apnea followed by recovery, against a background of no or variable myasthenic symptoms without dyspnea. One sib without myasthenic symptoms and one sib who only had mild ptosis died previously during febrile episodes. Studies reported by us elsewhere traced the proband's illness to mutations in choline acetyltransferase. Here, we describe in detail the morphologic investigations and electrophysiologic findings, which point to a presynaptic defect in acetylcholine resynthesis or vesicular filling, in the proband. Analysis of DNA from a sib who previously died of sudden infant death syndrome revealed the same choline acetyltransferase mutation. Thus, mutations in choline acetyltransferase may be a cause of sudden infant death syndrome as, theoretically, could other presynaptic myasthenic disorders.

摘要

婴儿猝死综合征有多种病因。一些先天性肌无力综合征可通过呼吸暂停导致婴儿猝死综合征,但其病因频率尚不清楚。我们在此报告一名年轻患者,在无或有变化的肌无力症状且无呼吸困难的背景下,突发呼吸危机,最终导致呼吸暂停,随后恢复。一名无肌无力症状的同胞和一名仅有轻度上睑下垂的同胞此前在发热发作期间死亡。我们在其他地方报告的研究将先证者的疾病追溯到胆碱乙酰转移酶的突变。在此,我们详细描述了先证者的形态学检查和电生理结果,这些结果表明乙酰胆碱再合成或囊泡填充存在突触前缺陷。对一名先前死于婴儿猝死综合征的同胞的DNA分析显示了相同的胆碱乙酰转移酶突变。因此,胆碱乙酰转移酶的突变可能是婴儿猝死综合征的一个病因,理论上,其他突触前肌无力疾病也可能是病因。

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