Radiological features of familial Gorlin-Goltz syndrome
Identifieur interne : 003D32 ( Ncbi/Checkpoint ); précédent : 003D31; suivant : 003D33Radiological features of familial Gorlin-Goltz syndrome
Auteurs : Shruthi Hegde [Inde] ; Shishir Ram Shetty [Inde]Source :
- Imaging Science in Dentistry [ 2233-7822 ] ; 2012.
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.
Url:
DOI: 10.5624/isd.2012.42.1.55
PubMed: 22474649
PubMed Central: 3314839
Affiliations:
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<front><div type="abstract" xml:lang="en"><p>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.</p>
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