Suppr超能文献

儿童慢性脊髓性肌萎缩症。其遗传学问题真的解决了吗?

Chronic form of childhood spinal muscular atrophy. Are the problems of its genetics really solved?

作者信息

Hausmanowa-Petrusewicz I, Zaremba J, Borkowska J

出版信息

J Neurol Sci. 1979 Oct;43(2):317-27. doi: 10.1016/0022-510x(79)90124-2.

Abstract

The authors discuss the differences between the two large series of chronic childhood spinal muscular atrophies (SMA)--their own comprising 273 cases, and that of Pearn et al. comprising 141 cases. The main difference concerns the predominance of males in the clinically milder later-onset group in the present series. The data of Pearn et al. (1978a, b) are quite different. The reason for the discrepancies is apparently a different selection of material. The present material is highly selective in favour of chronic cases, and Kugelberg-Welander cases are well-represented, whereas the percentage of Kugelberg-Welander cases in the material of Pearn et al. was very small. Differences in selection also appear to be responsible for discordance in observations regarding influence of sex on the course of the disease. The present data seem to support the view that most of the cases revealing chronic forms of SMA (both mild and severe) are not distinct genetically. However, the possible existence of a distinct subgroup in which sex influence is strongly expressed is not excluded.

摘要

作者讨论了两组大型儿童慢性脊髓性肌萎缩症(SMA)病例之间的差异——他们自己的研究包含273例病例,以及Pearn等人的研究包含141例病例。主要差异在于在本研究系列中临床症状较轻的晚发型组中男性占优势。Pearn等人(1978a,b)的数据则大不相同。差异的原因显然是材料选择不同。本研究材料高度偏向慢性病例,库格尔贝格 - 韦兰德(Kugelberg-Welander)型病例有很好的代表性,而在Pearn等人的材料中库格尔贝格 - 韦兰德型病例的比例非常小。选择上的差异似乎也是关于性别对疾病进程影响的观察结果不一致的原因。目前的数据似乎支持这样一种观点,即大多数呈现慢性形式SMA(包括轻度和重度)的病例在基因上并无明显差异。然而,并不排除可能存在一个性别影响强烈表达的独特亚组。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验