Gorlin-Goltz Syndrome: Report of 4 Cases

Kerdoud, Ouassime and Slimani, Faical (2020) Gorlin-Goltz Syndrome: Report of 4 Cases. Asian Journal of Dental Sciences, 3 (4). pp. 47-54.

[thumbnail of Kerdoud342020AJDS61980.pdf] Text
Kerdoud342020AJDS61980.pdf - Published Version

Download (1MB)

Abstract

Gorlin-Goltz syndrome, also known as basal cell nevomatosis (CBN), is a rare inherited disorder belonging to the family of neurocristopathies or diseases caused by abnormalities of the neural ridges. We report the case of 4 patients, suffering from this syndrome, followed up in the stomatology and maxillofacial surgery service in Casablanca, including a familial form in two cases: a mother and her son and 2 isolated cases, followed and treated in our service of maxillofacial surgery of the August 20 hospital in Casablanca. A clinical, biological and radiological assessment was made followed by surgical treatment for the 3 patients, an anatomo-pathological examination and the establishment of a strict monitoring plan.

Item Type: Article
Subjects: Pustaka Library > Medical Science
Depositing User: Unnamed user with email support@pustakalibrary.com
Date Deposited: 22 Mar 2023 09:36
Last Modified: 05 Mar 2024 04:12
URI: http://archive.bionaturalists.in/id/eprint/366

Actions (login required)

View Item
View Item