Gorlin syndrome presenting with a unilateral ovarian fibroma in a 22-year-old woman: a case report

INTRODUCTION: Nevoid basal cell carcinoma syndrome, or Gorlin syndrome, is an inherited disorder characterized by malignancies of the skin and other organs, skeletal abnormalities, and congenital malformations. The syndrome follows an autosomal dominant inheritance pattern with a gene mutation local...

Descripción completa

Detalles Bibliográficos
Autores principales: Finch, Terence, Pushpanathan, Chitra, Brown, Krista, El-Gohary, Yasser
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3423051/
https://www.ncbi.nlm.nih.gov/pubmed/22691621
http://dx.doi.org/10.1186/1752-1947-6-148

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3423051/
https://www.ncbi.nlm.nih.gov/pubmed/22691621
http://dx.doi.org/10.1186/1752-1947-6-148

Ejemplares similares