Blau syndrome: a new kindred.
case_report · Level V
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- Record sourced from PubMed, PMID 12894082.
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Abstract
Blau syndrome is a rare condition typically defined by granulomatous arthritis, skin eruption, and uveitis occurring in the absence of lung or other visceral involvement. Other characteristic physical findings include synovial cysts and camptodactyly. We describe a new kindred demonstrating autosomal dominant inheritance and anticipation.
Medical subject headings
- Granuloma
- Synovial Cyst
- Uveitis