Radiological features of familial Gorlin-Goltz syndrome
Shruthi Hegde, Shishir Ram Shetty,
소속 상세정보
( Shruthi Hegde ) - Nitte University AB Shetty Memorial Institute of Dental Sciences Department of Oral Medicine and Radiology
( Shishir Ram Shetty ) - Nitte University AB Shetty Memorial Institute of Dental Sciences Department of Oral Medicine and Radiology
KMID : 1024020120420010055
Abstract
Gorlin-Goltz syndrome is an autosomal dominant disorder principally characterized by cutaneous basal cell carcinomas, multiple keratocystic odontogenic tumors, and skeletal anomalies. This syndrome may be diagnosed early by dentist because keratocystic odontogenic tumors are usually one of the first manifestations of the syndrome. Early diagnosis and treatment are of utmost importance in reducing the severity of long term sequelae of this syndrome. This report presents a rare event of Gorlin-Goltz syndrome occurring in a 39-year-old male and his 8-year-old daughter. The clinical and investigative features of this familial disorder has been described in detail.
키워드
Basal Cell Nevus Syndrome; Odontogenic Cysts; Skeletal Anomalies
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