1.
West China Journal of Stomatology
;
(6): 230-232, 2021.
Artigo
em Chinês
| WPRIM
| ID: wpr-878436
RESUMO
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.