Cherubism in a 12-year old Child; A Rare Case Report

M. Hiremath, S. Srinath, B. Balan, S SushmaH
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Abstract

Cherubism is a non-neoplastic, fibro-osseous, self-limiting, autosomal dominant disorder of the jaws. It is also called as familial fibrous dysplasia and familial multi-locular cystic lesion of the jaws. Its typical dento-facial deformities are caused by mutations in the SH3BP2 gene. The lesion regresses during puberty and the disease stabilizes after the growth period. But it leaves some facial deformity along with disturbances in occlusion. Cherubism may occur as an individual case or in multiple members of the same family, oftenly in multiple generations. Radiographic examination of the lesion shows bilateral multi-locular radiolucent areas.The aim of this case report is to present a case of 12-years old cherubic child, with its clinical and radiological features and discussion about the clinical outcome.This patient was diagnosed with Cherubism and being followed up periodically.
12岁儿童的天使崇拜;一例罕见病例报告
小天使病是一种非肿瘤性、纤维骨性、自限性、常染色体显性的颌骨疾病。它也被称为家族性纤维性发育不良和家族性颌骨多室囊性病变。其典型的牙面畸形是由SH3BP2基因突变引起的。病变在青春期消退,在生长期后病情稳定。但它会留下一些面部畸形以及咬合障碍。基路伯病可能发生在个体身上,也可能发生在同一家族的多个成员身上,通常发生在几代人身上。x线检查显示双侧多室透光区。本病例报告的目的是提出一个12岁的小天使儿童,其临床和放射学特征和讨论的临床结果。该患者被诊断为基路伯病,并定期随访。
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