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Osteomyelitis of Maxilla in Infantile Osteopetrosis: A Case Report with Review of Literature

Osteopetrosis is a rare genetic disorder that causes generalized sclerosis of bone due to a defect in bone resorption and remodeling. It is usually manifesting in two basic forms: An autosomal dominant benign form (osteopetrosis tarda) and an autosomal recessive malignant form (osteopetrosis congeni...

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Detalles Bibliográficos
Autores principales:	Balan, Anita, Girija, KL, Ranimol, P
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Jaypee Brothers Medical Publishers 2011
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030498/ https://www.ncbi.nlm.nih.gov/pubmed/27672251 http://dx.doi.org/10.5005/jp-journals-10005-1095

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