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Gorlin's Syndrome-A case report.
Article Dans Anglais | IMSEAR | ID: sea-153652
ABSTRACT
Gorlin's syndrome is a rare disorder transmitted as an autosomal dominant trait. Most common phenotypic expression of this syndrome is a basal cell carcinoma (BCC). It is characterized by multiple skin lesions on head and neck region. We present a case of49 year old male who presented with basal cell carcinoma at multiple sites simultaneously.

Texte intégral: Disponible Indice: IMSEAR (Asie du Sud-Est) langue: Anglais Année: 2000 Type: Article

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Texte intégral: Disponible Indice: IMSEAR (Asie du Sud-Est) langue: Anglais Année: 2000 Type: Article