Blau syndrome: Difference between revisions
New page: {{SI}} {{EH}} ==Overview== '''Blau syndrome''' is characterized by familial granulomatous arthritis, iritis, and skin granulomas, comprising an autosomal dominantly ... |
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'''Blau syndrome''' is characterized by familial granulomatous arthritis, iritis, and skin granulomas, comprising an [[autosomal dominant|autosomal dominantly]] inherited syndrome that overlaps both sarcoidosis and granuloma annulare.<ref name="Fitz2">Freedberg, et. al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw-Hill. ISBN 0071380760.</ref>{{rp|983}}<ref name="Andrews">James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. ISBN 0721629210.</ref>{{rp|149}} Restated, blau syndrome is a rare autosomal dominant disorder characterized by granulomatous polyarthritis, panuveitis, cranial neuropathies and exanthema.<ref name="pmid17223962">{{cite journal |author=Ferrero-Miliani L, Nielsen OH, Andersen PS, Girardin SE |title=Chronic inflammation: importance of NOD2 and NALP3 in interleukin-1beta generation |journal=Clin. Exp. Immunol. |volume=147 |issue=2 |pages=227–35 |year=2007 |month=February |pmid=17223962 |pmc=1810472 |doi=10.1111/j.1365-2249.2006.03261.x |url=}}</ref>{{rp|232}} | '''Blau syndrome''' is characterized by familial granulomatous arthritis, iritis, and skin granulomas, comprising an [[autosomal dominant|autosomal dominantly]] inherited syndrome that overlaps both sarcoidosis and granuloma annulare.<ref name="Fitz2">Freedberg, et. al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw-Hill. ISBN 0071380760.</ref>{{rp|983}}<ref name="Andrews">James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. ISBN 0721629210.</ref>{{rp|149}} Restated, blau syndrome is a rare autosomal dominant disorder characterized by granulomatous polyarthritis, panuveitis, cranial neuropathies and exanthema.<ref name="pmid17223962">{{cite journal |author=Ferrero-Miliani L, Nielsen OH, Andersen PS, Girardin SE |title=Chronic inflammation: importance of NOD2 and NALP3 in interleukin-1beta generation |journal=Clin. Exp. Immunol. |volume=147 |issue=2 |pages=227–35 |year=2007 |month=February |pmid=17223962 |pmc=1810472 |doi=10.1111/j.1365-2249.2006.03261.x |url=}}</ref>{{rp|232}} | ||
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Revision as of 23:00, 8 August 2012
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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
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