Gorlin syndrome. A case report.
Article
Dans Anglais
| 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.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
Sujet Principal:
Humains
/
Mâle
/
Naevomatose basocellulaire
/
Tumeurs de la mâchoire
/
Adulte
langue:
Anglais
Année:
2001
Type:
Article
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