Sacroiliitis and Polyarteritis Nodosa in a Patient with Familial Mediterranean Fever
Familial Mediterranean fever (FMF) is an autoinflammatory disorder with autosomal recessive inheritance, characterized by recurrent fever and episodes of serositis. The condition is known to be caused by mutations in the MEFV (Mediterranean FeVer) gene, located in the short arm of chromosome 16. Whi...
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2016-01-01
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Series: | Case Reports in Medicine |
Online Access: | http://dx.doi.org/10.1155/2016/5134546 |
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author | Yunus Ugan Atalay Doğru Hüseyin Şencan Mehmet Şahin Şevket Ercan Tunç |
author_facet | Yunus Ugan Atalay Doğru Hüseyin Şencan Mehmet Şahin Şevket Ercan Tunç |
author_sort | Yunus Ugan |
collection | DOAJ |
description | Familial Mediterranean fever (FMF) is an autoinflammatory disorder with autosomal recessive inheritance, characterized by recurrent fever and episodes of serositis. The condition is known to be caused by mutations in the MEFV (Mediterranean FeVer) gene, located in the short arm of chromosome 16. While more than 310 sequence variants in the MEFV gene have been described to date, the diagnosis is still established clinically. FMF may be accompanied by sacroiliitis and various forms of vasculitis. The most common forms of associated vasculitis are Henoch-Schonlein purpura and polyarteritis nodosa (PAN). We have presented here a fairly rare case of FMF, accompanied by both sacroiliitis and PAN. |
format | Article |
id | doaj-art-32c1407a67484b85b2af7469d7bca2a4 |
institution | Kabale University |
issn | 1687-9627 1687-9635 |
language | English |
publishDate | 2016-01-01 |
publisher | Wiley |
record_format | Article |
series | Case Reports in Medicine |
spelling | doaj-art-32c1407a67484b85b2af7469d7bca2a42025-02-03T06:01:35ZengWileyCase Reports in Medicine1687-96271687-96352016-01-01201610.1155/2016/51345465134546Sacroiliitis and Polyarteritis Nodosa in a Patient with Familial Mediterranean FeverYunus Ugan0Atalay Doğru1Hüseyin Şencan2Mehmet Şahin3Şevket Ercan Tunç4Faculty of Medicine, Department of Internal Medicine, Division of Rheumatology, Suleyman Demirel University, 32260 Isparta, TurkeyFaculty of Medicine, Department of Internal Medicine, Division of Rheumatology, Suleyman Demirel University, 32260 Isparta, TurkeyFaculty of Medicine, Department of Internal Medicine, Suleyman Demirel University, 32260 Isparta, TurkeyFaculty of Medicine, Department of Internal Medicine, Division of Rheumatology, Suleyman Demirel University, 32260 Isparta, TurkeyFaculty of Medicine, Department of Internal Medicine, Division of Rheumatology, Suleyman Demirel University, 32260 Isparta, TurkeyFamilial Mediterranean fever (FMF) is an autoinflammatory disorder with autosomal recessive inheritance, characterized by recurrent fever and episodes of serositis. The condition is known to be caused by mutations in the MEFV (Mediterranean FeVer) gene, located in the short arm of chromosome 16. While more than 310 sequence variants in the MEFV gene have been described to date, the diagnosis is still established clinically. FMF may be accompanied by sacroiliitis and various forms of vasculitis. The most common forms of associated vasculitis are Henoch-Schonlein purpura and polyarteritis nodosa (PAN). We have presented here a fairly rare case of FMF, accompanied by both sacroiliitis and PAN.http://dx.doi.org/10.1155/2016/5134546 |
spellingShingle | Yunus Ugan Atalay Doğru Hüseyin Şencan Mehmet Şahin Şevket Ercan Tunç Sacroiliitis and Polyarteritis Nodosa in a Patient with Familial Mediterranean Fever Case Reports in Medicine |
title | Sacroiliitis and Polyarteritis Nodosa in a Patient with Familial Mediterranean Fever |
title_full | Sacroiliitis and Polyarteritis Nodosa in a Patient with Familial Mediterranean Fever |
title_fullStr | Sacroiliitis and Polyarteritis Nodosa in a Patient with Familial Mediterranean Fever |
title_full_unstemmed | Sacroiliitis and Polyarteritis Nodosa in a Patient with Familial Mediterranean Fever |
title_short | Sacroiliitis and Polyarteritis Nodosa in a Patient with Familial Mediterranean Fever |
title_sort | sacroiliitis and polyarteritis nodosa in a patient with familial mediterranean fever |
url | http://dx.doi.org/10.1155/2016/5134546 |
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