Article
Two novel ADAR1 gene mutations in two patients with dyschromatosis symmetrical hereditaria from birth.
Molecular medicine reports - 1 Jun 2017
Zhou Qian, Zhang Linglin, Zhang Yunfeng, Luo Hao, Zhu Lude, Wang Peiru, Zhang Guolong, Wang Xiuli
Abstract excerpt
Dyschromatosis symmetrica hereditaria (DSH) is a rare type of pigmentary genodermatosis, which is autosomal dominantly inherited with high penetrance. The onset of DSH is typically during infancy or childhood. Cases of patients born with skin lesions have rarely been reported. Additionally, there have been few significant non‑cutaneous complications reported with DSH. The present study reported two sporadic cases...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.