| Literature DB >> 3072678 |
M Martínez-Lavín1, C Pineda, T Valdez, J C Cajigas, M Weisman, N Gerber, D Steigler.
Abstract
We describe seven patients with primary HOA and review 125 cases reported in the English, French, and German literature. The salient clinical features of primary HOA are: a bimodal distribution of disease onset with one peak during the first year of life and the other at age 15, a male predominance (nine to one), uncommon benign joint effusion, and a variety of skin abnormalities resulting from cutaneous hypertrophy or glandular dysfunction. We concluded that HOA is not a synovial disease. It is suggested that synovial effusions, when present, are perhaps a sympathetic reaction to the neighboring periostitis. Proposed diagnostic criteria for HOA, including digital clubbing and radiographic periostitis, appear 86% sensitive. The clinical features, age of onset, and sex distribution suggest that a genetically controlled growth promoting factor, different from growth hormone, plays a role in the pathogenesis of this syndrome.Entities:
Mesh:
Year: 1988 PMID: 3072678 DOI: 10.1016/0049-0172(88)90017-0
Source DB: PubMed Journal: Semin Arthritis Rheum ISSN: 0049-0172 Impact factor: 5.532