| Literature DB >> 33834681 |
Zi-Yi Tian1, Wen Ma1, Zhi-Yue Zhao1, Ming Li1.
Abstract
Basal cell nevus syndrome (BCNS), also known as Gorlin-Goltz syndrome, is a rare autosomal dominant genetic disease. It is thought to be caused by a mutation in the PTCH1 gene, and its incidence is 1/57 000 to 1/256 000. The case of a 7-year-old patient with BCNS and Duchenne muscular dystrophy was reported in this paper.Entities:
Keywords: Duchenne muscular dystrophy; basal cell nevus syndrome; odontogenic keratocyst
Mesh:
Year: 2021 PMID: 33834681 PMCID: PMC8055780 DOI: 10.7518/hxkq.2021.02.017
Source DB: PubMed Journal: Hua Xi Kou Qiang Yi Xue Za Zhi ISSN: 1000-1182