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.
Research Article: Journal of Clinical Medicine and Therapeutics
Research Article: Journal of Clinical Medicine and Therapeutics
Commentary: Journal of Clinical Medicine and Therapeutics
Commentary: Journal of Clinical Medicine and Therapeutics
Case Report: Journal of Clinical Medicine and Therapeutics
Case Report: Journal of Clinical Medicine and Therapeutics
ScientificTracks Abstracts: Journal of Universal Surgery
ScientificTracks Abstracts: Journal of Universal Surgery
Posters & Accepted Abstracts: International Journal of Anesthesiology & Pain Medicine
Posters & Accepted Abstracts: International Journal of Anesthesiology & Pain Medicine
Posters & Accepted Abstracts: Journal of Pediatric Care
Posters & Accepted Abstracts: Journal of Pediatric Care
Posters & Accepted Abstracts: Journal of Obesity & Eating Disorders
Posters & Accepted Abstracts: Journal of Obesity & Eating Disorders
Journal of Clinical Medicine and Therapeutics received 69 citations as per Google Scholar report