Blau syndrome
WikiDoc Resources for Blau syndrome |
Articles |
---|
Most recent articles on Blau syndrome Most cited articles on Blau syndrome |
Media |
Powerpoint slides on Blau syndrome |
Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Blau syndrome at Clinical Trials.gov Trial results on Blau syndrome Clinical Trials on Blau syndrome at Google
|
Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Blau syndrome NICE Guidance on Blau syndrome
|
Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Patient resources on Blau syndrome Discussion groups on Blau syndrome Patient Handouts on Blau syndrome Directions to Hospitals Treating Blau syndrome Risk calculators and risk factors for Blau syndrome
|
Healthcare Provider Resources |
Causes & Risk Factors for Blau syndrome |
Continuing Medical Education (CME) |
International |
|
Business |
Experimental / Informatics |
Overview
Blau syndrome is characterized by familial granulomatous arthritis, iritis, and skin granulomas, comprising an autosomal dominantly inherited syndrome that overlaps both sarcoidosis and granuloma annulare.[1]:983[2]:149 Restated, blau syndrome is a rare autosomal dominant disorder characterized by granulomatous polyarthritis, panuveitis, cranial neuropathies and exanthema.[3]:232
References
- ↑ Freedberg, et. al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0071380760.
- ↑ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0721629210.
- ↑ Ferrero-Miliani L, Nielsen OH, Andersen PS, Girardin SE (2007). "Chronic inflammation: importance of NOD2 and NALP3 in interleukin-1beta generation". Clin. Exp. Immunol. 147 (2): 227–35. doi:10.1111/j.1365-2249.2006.03261.x. PMC 1810472. PMID 17223962. Unknown parameter
|month=
ignored (help)