Gorlin's Syndrome-A case report.
Article
in En
| IMSEAR
| ID: sea-153652
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.
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Index:
IMSEAR
Language:
En
Year:
2000
Type:
Article