Autosomal-dominant osteopetrosis: An incidental finding
Author(s) -
Maria Rajathi,
RaviDavid Austin,
Philips Mathew,
CSaravana Bharathi,
Kumar Chandan Srivastava
Publication year - 2010
Publication title -
indian journal of dental research
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.277
H-Index - 43
eISSN - 1998-3603
pISSN - 0970-9290
DOI - 10.4103/0970-9290.74234
Subject(s) - osteopetrosis , medicine , osteochondrodysplasia , disease , osteomyelitis , osteoclast , pathology , immunology , receptor
Osteopetrosis is a descriptive term that refers to a group of rare, heritable disorders of the skeleton. Osteopetrotic conditions vary greatly in their presentation and severity, from just as an incidental finding on radiographs to causing life-threatening complications such as bone marrow suppression. It is caused by failure of osteoclast development and function. Osteopetrosis can be inherited as autosomal-recessive, autosomal-dominant or as X-linked traits, with the most severe forms being the autosomal-recessive ones. The severity of the disease is mild to moderate in the autosomal-dominant forms, with normal life expectancy. Diagnosis is largely based on clinical and radiographic evaluation. The present paper reports a case of autosomal-dominant osteopetrosis complicated by osteomyelitis with a short review of the condition.
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