Familial Mediterranean fever (FMF) is a hereditary inflammatory disorder. FMF is an auto inflammatory disease caused by mutations in Mediterranean fever gene, which encodes a 781–amino acid protein called pyrin. While all ethnic groups are susceptible to FMF, it generally occurs more in people of Mediterranean origin—including Sephardic Jews, Mizrahi Jews, Ashkenazi Jews, Armenians, Azerbaijanis, Arabs, Kurds, Greeks, Turks and Italians. The disorder has been assigned various names such as familial paroxysmal polyserositis, periodic peritonitis, recurrent polyserositis, benign paroxysmal peritonitis, periodic disease or periodic fever, Reimann periodic disease or Reimann syndrome, Siegal-Cattan-Mamou disease, and Wolff periodic disease.
Young Research Forum: Journal of Clinical Medicine and Therapeutics
Young Research Forum: Journal of Clinical Medicine and Therapeutics
Review Article: Journal of Clinical Medicine and Therapeutics
Review Article: Journal of Clinical Medicine and Therapeutics
Posters & Accepted Abstracts: Archives of Medicine
Posters & Accepted Abstracts: Archives of Medicine
ScientificTracks Abstracts: Dentistry and Craniofacial Research
ScientificTracks Abstracts: Dentistry and Craniofacial Research
Posters & Accepted Abstracts: Dentistry and Craniofacial Research
Posters & Accepted Abstracts: Dentistry and Craniofacial Research
Posters & Accepted Abstracts: Journal of Vascular and Endovascular Therapy
Posters & Accepted Abstracts: Journal of Vascular and Endovascular Therapy
Journal of Clinical Medicine and Therapeutics received 95 citations as per Google Scholar report