Cherubism: a rare case report with literature review

Cherubism is an autosomal dominant disorder caused by a mutation of the gene encoding the binding protein SH3BP2. However, non-hereditary forms are observed, probably related to a de novo mutation. It is clinically manifested by an enlargement or a deformation of the jaw associated with a malpositio...

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Bibliographic Details
Main Authors: A. Lahfidi, MD, W.M. Traore, MD, I.D. Diallo, MD, N. Lrhorfi, MD, S. Elhaddad, MD, N. Allali, MD, L. Chat, MD
Format: Article
Language:English
Published: Elsevier 2022-10-01
Series:Radiology Case Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1930043322006100