Gorlin-Goltz Syndrome – A Rare Case Entity in Young Child
| Autor: | Shovita Mondal, Nikil Kumar Jain, Abhishek Dutta, Nishant, Abhijit Dutta, Moushumi Shil, Suman Sen |
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| Jazyk: | angličtina |
| Rok vydání: | 2024 |
| Předmět: | |
| Zdroj: | Prague Medical Report, Vol 125, Iss 1, Pp 69-78 (2024) |
| Druh dokumentu: | article |
| ISSN: | 2336-2936 1214-6994 23362936 |
| DOI: | 10.14712/23362936.2024.7 |
| Popis: | Gorlin-Goltz syndrome (GGS) is an infrequent multisystemic disease with an autosomal dominant trait, which depicted presence of numerous basal cell carcinoma in conjunction with multiorgan abnormalities. This syndrome may be diagnosed early by a dentist by routine radiographic exams in the first decade of life, since the keratocystic odontogenic tumour are usually one of the first manifestations of the syndrome. This article includes a case report of the GGS with regard to its history, incidence, etiology, features, investigations, diagnostic criteria, keratocystic odontogenic tumour and treatment modalities. |
| Databáze: | Directory of Open Access Journals |
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