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常染色体显性遗传的多发性咖啡牛奶斑与神经纤维瘤病1型:非连锁证据

Autosomal dominant multiple café-au-lait spots and neurofibromatosis-1: evidence of non-linkage.

作者信息

Charrow J, Listernick R, Ward K

机构信息

Division of Genetics, Children's Memorial Hospital, Chicago, Illinois 60614.

出版信息

Am J Med Genet. 1993 Mar 1;45(5):606-8. doi: 10.1002/ajmg.1320450518.

Abstract

Multiple café-au-lait spots have been observed in successive generations of several families without any other manifestations of neurofibromatosis (NF) or any other systemic disorder. The café-au-lait spots in these families segregate as an autosomal dominant trait. The relationship (if any) between the gene for this trait and the NF-1 gene has previously been unknown. We describe a family with five individuals spanning four generations with dominantly inherited café-au-lait spots, without any other stigmata of NF-1. Linkage analysis with probes proximal, distal, and within the NF-1 gene indicate that the trait in this family is not linked to NF-1. We propose that this condition be called Familial Café-Au-Lait Spots (FCAL) to distinguish it from the neurofibromatosis syndromes.

摘要

在几个家族的连续几代人中都观察到了多个咖啡牛奶斑,且没有任何神经纤维瘤病(NF)或任何其他全身性疾病的其他表现。这些家族中的咖啡牛奶斑作为常染色体显性性状进行分离。此前,该性状的基因与NF-1基因之间的关系(如果存在)尚不清楚。我们描述了一个家族,该家族四代中有五人具有显性遗传的咖啡牛奶斑,没有任何NF-1的其他特征。使用NF-1基因近端、远端和内部的探针进行连锁分析表明,该家族中的性状与NF-1不连锁。我们建议将这种病症称为家族性咖啡牛奶斑(FCAL),以将其与神经纤维瘤病综合征区分开来。

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