Suppr超能文献

Piebaldism and neurofibromatosis type 1: family report.

作者信息

Duarte Ana Filipa, Mota Alberto, Baudrier Teresa, Morais Paulo, Santos António, Cerqueira Rita, Tavares Purificação, Azevedo Filomena

机构信息

Department of Dermatology, Hospital de São João, EPE, Porto, Portugal.

出版信息

Dermatol Online J. 2010 Jan 15;16(1):11.

Abstract

Piebaldism is a rare disorder present at birth and inherited as an autosomal dominant trait. It results from a mutation in the c-kit proto-oncogene and is associated with a defect in the migration and differentiation of melanoblasts from the neural crest. Clinical manifestations and phenotypic severity strongly correlates with the site of mutation within the KIT gene. Here we report a 3-year-old boy and his 33-year-old father with leukoderma and poliosis associated with clinical criteria for Neurofibromatosis type 1. Genetic study of both revealed a p.Gly610Asp mutation in the KIT gene. This familiar mutation has not yet been reported in the literature. There are rare reports of piebaldism in association with neurofibromatosis type I.

摘要

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