Gorlin syndrome. A case report.
Artículo
en Inglés
| IMSEAR
| ID: sea-51394
ABSTRACT
Gorlin's syndrome is a genetic disorder of autosomal dominant inheritance with high penetrance and variable expression. It embraces a constellation of many organs principally affects the skin, skeleton, and endocrine and nervous system. A rare case is reported to illustrate the features of Gorlin's syndrome without the features of basal cell carcinoma and to emphasize the need for early recognition and careful follow up by the dentist prevent severe sequelae.
Texto completo:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Asunto principal:
Humanos
/
Masculino
/
Síndrome del Nevo Basocelular
/
Neoplasias Maxilomandibulares
/
Adulto
Idioma:
Inglés
Año:
2001
Tipo del documento:
Artículo
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