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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...
Autores principales: | Sharma, Ankit, Ingole, Snehal N, Deshpande, Mohan D, Kazi, Noaman, Meshram, Deepashree, Ranadive, Pallavi |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Jaypee Brothers Medical Publishers
2020
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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 |
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