Basal cell nevus syndrome with Duchenne muscular dystrophy: a case report / 华西口腔医学杂志
West China Journal of Stomatology
; (6): 230-232, 2021.
Article
Dans Zh
| WPRIM
| ID: wpr-878436
Responsable en Bibliothèque :
WPRO
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.
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Naevomatose basocellulaire
/
Myopathie de Duchenne
/
Mutation
Limites du sujet:
Child
/
Humans
langue:
Zh
Texte intégral:
West China Journal of Stomatology
Année:
2021
Type:
Article