A Rare Case of Osteoclast-poor Osteopetrosis (RANKL Mutation) with Recurrent Osteomyelitis of Mandible: A Case Report.
Sharma A, Ingole SN, Deshpande MD, Kazi N, Meshram D, Ranadive P.
Sharma A, et al.
Int J Clin Pediatr Dent. 2020 Nov-Dec;13(6):717-721. doi: 10.5005/jp-journals-10005-1835.
Int J Clin Pediatr Dent. 2020.
PMID: 33976500
Free PMC article.
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 defe …
Osteopetrosis (OP) is a group of rare genetic bone disorders. Osteoclast-poor form of osteopetrosis is much rarer in humans and repre …