A Rare Case of Osteoclast-poor Osteopetrosis (RANKL Mutation) with Recurrent Osteomyelitis of Mandible: A Case Report

Osteopetrosis (OP) is a group of rare genetic bone disorders. Osteoclast-poor form of osteopetrosis is much rarer in humans and represents a small percentage of the total cases of autosomal recessive osteopetrosis presenting with impaired bone remodeling due to defective osteoclastic activity and is...

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Detalles Bibliográficos
Autores principales: Sharma, Ankit, Ingole, Snehal N, Deshpande, Mohan D, Kazi, Noaman, Meshram, Deepashree, Ranadive, Pallavi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Jaypee Brothers Medical Publishers 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060946/
https://www.ncbi.nlm.nih.gov/pubmed/33976500
http://dx.doi.org/10.5005/jp-journals-10005-1835

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060946/
https://www.ncbi.nlm.nih.gov/pubmed/33976500
http://dx.doi.org/10.5005/jp-journals-10005-1835

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