Gorlin-goltz syndrome: a report of two clinical cases with diagnosis and treatment at hospital level
Gorlin-Goltz syndrome, also known as nevoid basal cell carcinoma syndrome, is a rare hereditary autosomal dominant condition, with high penetrance and variable expressivity. The aim of this study is to report 2 cases diagnosed at emergency hospital units with the specialty of maxillofacial surgery and traumatology. The first refers to a 10-year-old patient who sought consultation due to an expressive increase in the maxilla volume with panoramic radiography evidencing multiple unilocular radiolucent images in the gnathic bones.
Source: Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics - Category: ENT & OMF Authors: Kelly Tambasco Bezerra, Gabriela Later ça Da Silva Abreu, Jackeline Nogueira De Paula Barros, Regina Celia De Souza Jesus Rangel, Alexandre Moreira De Moraes, Fábio Ramôa Pires, Águida Maria Menezes Aguiar Miranda Source Type: research
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