منابع مشابه
Osteopetrosis Presenting with Neonatal Thrombocytopenia: A Case Report
Background: Osteopetrosisis an inherited and rare bone disease, characterized by the impairment ofbone modeling and remodeling and the failure of osteoclasts to resorb bone. It also results in skeletal fragility despite increased bone mass, and may cause hematopoietic insufficiency, disturbed tooth eruption, nerve entrapment syndromes, and growth impairment. The infantile form of the disease is...
متن کاملOsteopetrosis Complicated by Maxillary Osteomyelitis: A Case Report
Introduction: Maxillary osteomyelitis is a rare phenomenon. If it occurs, evaluation for underlying disease especially osteopetrosis must be considered. Osteomyelitis occurs as a complication in 10% of the cases of osteopetrosis. Case report: This is a case report of maxillary osteomyelitis presented in a 15-year old boy with osteopetrosis. In this case, the disease represented mainly with ...
متن کاملA Case Report of Malignant Infantile Osteopetrosis
BACKGROUND Malignant infantile osteopetrosis (MIOP) presents early in life with extreme sclerosis of the skeleton and reduction of bone marrow spaces. Since there is a defect in the bone marrow, the disease can cause anemia, extramedullary hematopoiesis secondary to anemia leading to hepatosplenomegaly, cranial nerves compression and severe growth failure. This disorder is often lethal within t...
متن کاملMaxillary Osteomyelitis Secondary To Osteopetrosis – A Rare Case Report
Osteomyelitis of the mandible at a young age may occur as a complication of immunocompromised status or bone disorders. Osteomyelitis rarely occurs in the maxilla due to thin bone and collateral blood supply of the maxillary bone. We report here, a rare case of maxillary osteomyelitis that led to the diagnosis of the underlying condition of osteopetrosis. The clinical and radiographical feature...
متن کاملDebridement in chronic osteomyelitis with benign osteopetrosis: A case report
Osteopetrosis is a rare bone disease caused by metabolic imbalances as a result of genetic mutations. For instance, autosomal dominant osteopetrosis is caused by a missense mutation of the C1CN7 gene. This was first reported in 1904 and is thought to be caused by osteoclastic dysfunction and an impaired bone resorption ability. An accumulation of cortical bone mass during the remodeling of the ...
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ژورنال
عنوان ژورنال: International Journal of Medical & Dental Case Reports
سال: 2016
ISSN: 2394-7152
DOI: 10.15713/ins.ijmdcr.33