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[晚发型婴儿型肌萎缩的临床分析]

[Clinical analysis of late infantile form of muscular atrophy].

作者信息

Stemler T

出版信息

Neurol Neurochir Pol. 1979 Jul-Aug;13(4):377-82.

PMID:481689
Abstract

Clinical analysis of 47 cases of late infantile spinal muscular atrophy is reported. In 25.5% of cases mothers reported weak fetal movements in pregnancy and low muscular tonus after birth, these signs predicted early manifestation of the disease. In 89,2% of cases the first signs of the disease appeared within the first 3 years of life. Delayed motor development in infancy was observed in 59.6%. Immobilization developed between the ages of 2 and 18 years, usually after 7 years of disease duration, and it was not correlated with the age of onset of the first signs of the disease. Mental development was normal in 81.5% of cases. Familial character of the disease was found in 51.1% of cases and in some of them intrafamilial variability was observed.

摘要

报告了47例晚发性婴儿脊髓性肌萎缩症的临床分析。在25.5%的病例中,母亲报告孕期胎动弱且出生后肌张力低,这些体征预示着疾病的早期表现。在89.2%的病例中,疾病的首发体征出现在生命的前3年内。59.6%的病例在婴儿期出现运动发育迟缓。2至18岁之间出现固定状态,通常在疾病持续7年后,且与疾病首发体征的发病年龄无关。81.5%的病例智力发育正常。51.1%的病例发现有家族性特征,其中一些观察到家族内变异性。

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