Síndrome de GorlinManifestaciones clínicas y su relación con alteraciones genéticas en el cromosoma 9
- Abel García García
- María Mercedes Suárez Cunqueiro
- Ángel Carracedo Álvarez
- José Manuel Gándara Rey
- José Ramón Antúnez López
- Arturo Bilbao Alonso
ISSN: 1130-0558
Ano de publicación: 1997
Volume: 19
Número: 4
Páxinas: 210-216
Tipo: Artigo
Outras publicacións en: Revista española de cirugía oral y maxilofacial: Publicación Oficial de la Sociedad Española de Cirugía Oral y Maxilofacial
Resumo
Basal cell nevus syndrome (Gorlin syndrome) is an autosomal dominant condition with highly variable manifestations, the most frequent being carcinoma of nevoid basal cells of the skin, odontogenic keratocysts of the jaw, and other bone abnormalities. Here, we report a case of basal cell nevus syndrome. The patient was characterized on the basis of clinical, radiological and anatomical-pathological examination, and a genetic analysis was also performed. We discuss our findings and compare them with those of other authors.