Familial expansile osteolysis

Disease Export to PDF
Name:
Familial expansile osteolysis
Description:
A rare primary bone dysplasia characterized by abnormal bone metabolism with bone pain, deformity, pathological fractures, early conductive hearing loss, and dental abnormalities. Focal bone lesions are typically found in the appendicular skeleton and consist of progressively expanding lytic areas, while generalized disordered bone modeling and altered trabecular pattern are the result of the multifocal, progressive nature of the disease. Age of onset is variable, mode of inheritance is autosomal dominant.
ORPHAcode:
85195
Synonyms:
Hereditary expansile polyostotic osteolytic dysplasia
McCabe disease
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Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14