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Article

A novel mutation in TNFRSF11A gene causes pediatric osteopetrosis: case report.

BMC surgery - 28 May 2021

Xu You, Yu Xiaoyan, Huang Mengjie

Abstract excerpt

BACKGROUND: Osteopetrosis is a rare inherited bone disorder affected individual by osteoclast disfunction and increasing bone density. Surgery was taken for histological examination of the specimen and evidence of malignancy was not found. Finally, X-ray and gene detection lead to the diagnosis. CASE PRESENTATION: We report a 10-year-old girl with two years history of pus rhinorrhea, nasal obstruction and smelly...

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Identifiers

PMID: 34049530
DOI: 10.1186/s12893-021-01266-4
PMCID: PMC8162000

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