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Radiological features of familial Gorlin-Goltz syndrome

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Radiological features of familial Gorlin-Goltz syndrome

Auteurs : Shruthi Hegde [Inde] ; Shishir Ram Shetty [Inde]

Source :

Imaging Science in Dentistry [ 2233-7822 ] ; 2012.

RBID : PMC:3314839

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:

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3314839

DOI: 10.5624/isd.2012.42.1.55
PubMed: 22474649
PubMed Central: 3314839

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PMC:3314839

Le document en format XML

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Radiological features of familial Gorlin-Goltz syndrome

Radiological features of familial Gorlin-Goltz syndrome

Source :

Abstract

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