Gorlin syndrome: A case report.
J Indian Soc Pedod Prev Dent
;
2005 Oct-Dec; 23(4): 198-203
Article
in English
| IMSEAR
| ID: sea-114663
ABSTRACT
Gorlin syndrome is an autosomal dominant inherited condition that exhibits high penetrance and variable expressivity. It is characterized mainly by Basal cell carcinomas, Odontogenic keratocysts and skeletal anomalies. However, medical literature documents both common and lesser known manifestations of the disorder involving the skin, central nervous system, skeletal system etc. Diagnosis of the syndrome in childhood is basically through oral abnormalities. A case of Gorlin syndrome has been reported here, with review of literature.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Language:
English
Journal:
J Indian Soc Pedod Prev Dent
Journal subject:
Dentistry
Year:
2005
Type:
Article
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