Gorlin-Goltz syndrome, commonly known as basal cell nevomatosis (CBN), is a rare genetic ailment that belongs to the neurocristopathies family of disorders characterised by abnormalities of the neural ridges. We present the case of four patients with this syndrome who were followed up in Casablanca's stomatology and maxillofacial surgery service, including a familial form in two cases: a mother and her son, and two isolated cases, all of whom were followed and treated in our maxillofacial surgery service at the August 20 hospital. Following a clinical, biological, and radiological evaluation, surgical treatment for the three patients, an anatomo-pathological investigation, and the implementation of a stringent monitoring plan were carried out.
Please click here : https://journalajds.com/index.php/AJDS/article/view/30129
No comments:
Post a Comment