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VOL. 6, ISSUE 2 (2024)
Gorlin goltz syndrome: A case report and literature review
Authors
Priyanka Bit, Sohini Halder, Preety Sodhani, Prakhar Bhardwaj, Pradip Kumar Giri
Abstract
A rare multisystemic disease, Gorlin-Goltz
syndrome (GGS) is an autosomal dominant hereditary disorder characterised by
multiple basal cell nevi carcinomas, multiple keratocystic odontogenic tumours
(KCOT) in the jaws, and abnormalities in the skeletal structure. Gorlin-Goltz
syndrome should be diagnosed as early as possible because it can develop into
aggressive basal cell carcinomas and neoplasias. Seldom have cases of
Gorlin-Goltz syndrome been documented in eastern Indian subcontinent. This
article offers a thorough literature analysis on the illness and details the
case of a 15-year-old girl patient with Gorlin-Goltz syndrome.
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Pages:14-16
How to cite this article:
Priyanka Bit, Sohini Halder, Preety Sodhani, Prakhar Bhardwaj, Pradip Kumar Giri "Gorlin goltz syndrome: A case report and literature review". International Journal of Dental Research, Vol 6, Issue 2, 2024, Pages 14-16
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