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[多发性硬化症的家族易感性]

[Familial predisposition to multiple sclerosis].

作者信息

Turpin J C, Dubois D, Delasnerie-Laupretre N

出版信息

Rev Neurol (Paris). 1986;142(5):509-16.

PMID:3787053
Abstract

Seven families were studied to evaluate the influence of genetic factors in MS and its transmissibility. The disease was associated with some B7 and/or DR2 alleles in relation to the susceptibility gene in all but one case. This association was always transmissible conjointly. The carrier haplotype conditions disease manifestations and its prognosis, favorable in this series, but it is not sufficient to promote the onset of the disease. This requires a triggering factor with sometimes disorders affecting 3 generations as demonstrated by the analysis of one family. Therefore there is not a genic heredity but a predisposition heredity. Possible associations of MS with other morbid states such as insulin-dependent diabetes must be considered when counselling families.

摘要

研究了七个家庭,以评估遗传因素在多发性硬化症(MS)中的影响及其遗传性。除了一个病例外,在所有病例中,该疾病都与一些与易感基因相关的B7和/或DR2等位基因有关。这种关联总是共同遗传的。携带单倍型决定疾病表现及其预后,在本系列中预后良好,但不足以引发疾病。这需要一个触发因素,有时这种紊乱会影响三代人,正如对一个家庭的分析所示。因此,不存在基因遗传,而是一种易感性遗传。在为家庭提供咨询时,必须考虑MS与其他病态如胰岛素依赖型糖尿病之间可能的关联。

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