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等位基因体细胞突变可能解释血管性双胎痣。

Allelic somatic mutations may explain vascular twin nevi.

作者信息

Happle R

机构信息

Department of Dermatology, University of Nijmegen, The Netherlands.

出版信息

Hum Genet. 1991 Jan;86(3):321-2. doi: 10.1007/BF00202421.

Abstract

Vascular twin nevi, i.e., telangiectatic nevus and nevus anemicus occurring together and adjacent to each other, can be explained as twin spots resulting from a somatic recombination. It is so far unclear, however, whether the postulated underlying autosomal recessive mutations are allelic. This problem can be approached by studying another cutaneous phenotype, phacomatosis pigmentovascularis. Within this diagnosis, several authors have reported the simultaneous occurrence of three different birthmarks, viz., a pigmentary nevus, a telangiectatic nevus and a nevus anemicus. These cases can also be explained as a twin-spot phenomenon, provided two of these nevi are considered allelic traits. The two vascular nevi are most probably allelic, whereas the pigmentary nevus may be a nonallelic component of this syndrome. In conclusion, phacomatosis pigmentovascularis provides circumstantial evidence suggesting allelism of somatic mutations giving rise to two different vascular nevi.

摘要

血管性双痣,即毛细血管扩张痣和贫血痣同时出现且彼此相邻,可解释为体细胞重组产生的双斑。然而,目前尚不清楚所假定的潜在常染色体隐性突变是否为等位基因。这个问题可以通过研究另一种皮肤表型——色素血管性斑痣性错构瘤病来解决。在这个诊断范围内,几位作者报告了三种不同胎记同时出现的情况,即色素痣、毛细血管扩张痣和贫血痣。如果将其中两种痣视为等位基因性状,这些病例也可以解释为双斑现象。这两种血管痣很可能是等位基因,而色素痣可能是该综合征的非等位基因成分。总之,色素血管性斑痣性错构瘤病提供了间接证据,表明导致两种不同血管痣的体细胞突变存在等位基因关系。

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