[EN]: Gorlin syndrome is a rare autosomal dominant disease caused by mutations in the sonic hedgehog signaling pathway. Of particular importance is the PTCH1 gene. The disease is characterized by the development of multiple basal cell carcinomas at young ages. These tumors may present with other skin manifestations such as palmoplantar pits and with extracutaneous manifestations such as odontogenic keratocysts and medulloblastoma. Although the dermatologist may be key for recognizing clinical suspicion of the syndrome, a multidisciplinary team is usually necessary for diagnosis, treatment, and follow-up. Skin treatment may be complicated due to the large number of basal cell carcinomas and the extent of involvement. In recent years, new dru...
Gorlin syndrome is a rare autosomal dominant disorder exhibiting high penetrance and variable expres...
ResumenIntroducción/objetivoEl síndrome de Gorlin-Goltz (SGG) es un trastorno hereditario autosómico...
Background: Gorlin-Goltz syndrome, also known as nevoid basal cell carcinoma syndrome, is a rare gen...
RESUMEN El síndrome Gorlin (SG) es una condición genética, con patrón de herencia autosómico dominan...
El síndrome Gorlin (SG) es una condición genética, con patrón de herencia autosómico dominante, con ...
Gorlin-Goltz syndrome or nevoid basal cell carcinoma syndrome is a rare hereditary autosomal-dominan...
BACKGROUND Gorlin syndrome, also known as the basal cell nevus syndrome (OMIM #109400), is a rare...
Le syndrome de Gorlin est une maladie rare caractérisée par de nombreuses anomalies du développement...
[ES]El síndrome de Gorlin es una enfermedad infrecuente de herencia autosómica dominante producida p...
A síndrome de Gorlin-Goltz é uma patologia hereditária, rara, autossómica dominante de penetrância c...
Le syndrome de Gorlin et Goltz est une affection héréditaire, à transmission autosomique dominante, ...
Le syndrome de Gorlin-Goltz ou naevomatose basocellulaire est une affection héréditaire, ...
Copyright © 2012 Padma Pandeshwar et al. This is an open access article distributed under the Creati...
Gorlin-Goltz syndrome, also known as nevoid basal cell carcicoma syndrome, comes into being due to a...
[Background]: Naevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant disorder charac...
Gorlin syndrome is a rare autosomal dominant disorder exhibiting high penetrance and variable expres...
ResumenIntroducción/objetivoEl síndrome de Gorlin-Goltz (SGG) es un trastorno hereditario autosómico...
Background: Gorlin-Goltz syndrome, also known as nevoid basal cell carcinoma syndrome, is a rare gen...
RESUMEN El síndrome Gorlin (SG) es una condición genética, con patrón de herencia autosómico dominan...
El síndrome Gorlin (SG) es una condición genética, con patrón de herencia autosómico dominante, con ...
Gorlin-Goltz syndrome or nevoid basal cell carcinoma syndrome is a rare hereditary autosomal-dominan...
BACKGROUND Gorlin syndrome, also known as the basal cell nevus syndrome (OMIM #109400), is a rare...
Le syndrome de Gorlin est une maladie rare caractérisée par de nombreuses anomalies du développement...
[ES]El síndrome de Gorlin es una enfermedad infrecuente de herencia autosómica dominante producida p...
A síndrome de Gorlin-Goltz é uma patologia hereditária, rara, autossómica dominante de penetrância c...
Le syndrome de Gorlin et Goltz est une affection héréditaire, à transmission autosomique dominante, ...
Le syndrome de Gorlin-Goltz ou naevomatose basocellulaire est une affection héréditaire, ...
Copyright © 2012 Padma Pandeshwar et al. This is an open access article distributed under the Creati...
Gorlin-Goltz syndrome, also known as nevoid basal cell carcicoma syndrome, comes into being due to a...
[Background]: Naevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant disorder charac...
Gorlin syndrome is a rare autosomal dominant disorder exhibiting high penetrance and variable expres...
ResumenIntroducción/objetivoEl síndrome de Gorlin-Goltz (SGG) es un trastorno hereditario autosómico...
Background: Gorlin-Goltz syndrome, also known as nevoid basal cell carcinoma syndrome, is a rare gen...