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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...
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| Publicado en: | Int J Clin Pediatr Dent |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Jaypee Brothers Medical Publishers
2020
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8060946/ https://ncbi.nlm.nih.gov/pubmed/33976500 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5005/jp-journals-10005-1835 |
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