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A novel mutation in TNFRSF11A gene causes pediatric osteopetrosis: case report
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. CAS...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162000/ https://www.ncbi.nlm.nih.gov/pubmed/34049530 http://dx.doi.org/10.1186/s12893-021-01266-4 |