BIOMAT Database Logo BIOMAT Database Logo

[Familial Mediterranean fever and other hereditary recurrent inflammatory diseases]. 2005

Gilles Grateau

UI MeSH Term Description Entries
D010505 Familial Mediterranean Fever A group of HEREDITARY AUTOINFLAMMATION DISEASES, characterized by recurrent fever, abdominal pain, headache, rash, PLEURISY; and ARTHRITIS. ORCHITIS; benign MENINGITIS; and AMYLOIDOSIS may also occur. Homozygous or compound heterozygous mutations in marenostrin gene encoding PYRIN result in autosomal recessive transmission; simple heterozygous, autosomal dominant form of the disease also exists with mutations in the same gene. Mediterranean Fever, Familial,Periodic Disease,Periodic Disease, Wolff's,Wolff Periodic Disease,Wolff's Periodic Disease,Benign Paroxysmal Peritonitis,Familial Mediterranean Fever, Autosomal Dominant,Familial Mediterranean Fever, Autosomal Recessive,Familial Paroxysmal Polyserositis,Periodic Peritonitis,Polyserositis, Familial Paroxysmal,Polyserositis, Recurrent,Recurrent Polyserositis,Benign Paroxysmal Peritonitides,Disease, Periodic,Disease, Wolff Periodic,Disease, Wolff's Periodic,Diseases, Periodic,Familial Paroxysmal Polyserositides,Paroxysmal Peritonitides, Benign,Paroxysmal Peritonitis, Benign,Paroxysmal Polyserositides, Familial,Paroxysmal Polyserositis, Familial,Periodic Disease, Wolff,Periodic Disease, Wolffs,Periodic Diseases,Periodic Peritonitides,Peritonitides, Benign Paroxysmal,Peritonitides, Periodic,Peritonitis, Benign Paroxysmal,Peritonitis, Periodic,Polyserositides, Familial Paroxysmal,Polyserositides, Recurrent,Recurrent Polyserositides,Wolffs Periodic Disease
D003598 Cytoskeletal Proteins Major constituent of the cytoskeleton found in the cytoplasm of eukaryotic cells. They form a flexible framework for the cell, provide attachment points for organelles and formed bodies, and make communication between parts of the cell possible. Proteins, Cytoskeletal
D003937 Diagnosis, Differential Determination of which one of two or more diseases or conditions a patient is suffering from by systematically comparing and contrasting results of diagnostic measures. Diagnoses, Differential,Differential Diagnoses,Differential Diagnosis
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000071198 Pyrin A tripartite motif protein that consists of an N-terminal pyrin domain, a central coiled-coil region and B-box type ZINC FINGER, and C-terminal regions that mediate homotrimerization and interactions with other proteins (the B30.2/SPRY DOMAIN). It is expressed primarily by mature GRANULOCYTES and associates with the cytoskeleton in the perinuclear area as well as AUTOPHAGOSOMES, where it co-ordinates the assembly of AUTOPHAGY-RELATED PROTEINS and degradation of INFLAMMASOME components. It functions in INNATE IMMUNITY and INFLAMMATION; mutations in the Pyrin protein (MEFV) gene are associated with FAMILIAL MEDITERRANEAN FEVER. MEFV Protein,Marenostrin,Mediterranean Fever Protein,TRIM20 Protein

Related Publications

Gilles Grateau
Third International Conference on Familial Mediterranean Fever and Other Hereditary Inflammatory Disorders.
February 2003, The Israel Medical Association journal : IMAJ,
Gilles Grateau
Acute hepatitis in recurrent hereditary polyserositis (familial Mediterranean fever).
August 1994, Journal of tropical pediatrics,
Gilles Grateau
Recurrent hereditary polyserositis or familial Mediterranean fever: An overview.
September 1991, Annals of Saudi medicine,
Gilles Grateau
Update on Auto-Inflammatory Diseases and Familial Mediterranean Fever.
January 2016, The Israel Medical Association journal : IMAJ,
Gilles Grateau
Familial Mediterranean fever presenting as recurrent acute pelvic inflammatory disease.
May 2003, Obstetrics and gynecology,
Gilles Grateau
[Recurrent abdominal pain and fever: familial Mediterranean fever].
April 1992, Medizinische Klinik (Munich, Germany : 1983),
Gilles Grateau
Familial Mediterranean fever (recurrent hereditary polyserositis) in children: analysis of 88 cases.
June 1989, European journal of pediatrics,
Gilles Grateau
Familial Mediterranean fever--renal involvement by diseases other than amyloid.
February 1999, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association,
Gilles Grateau
[Recurrent pericarditis in familial Mediterranean fever].
May 1995, Harefuah,
Gilles Grateau
[Familial Mediterranean fever (or recurrent polyserositis)].
November 1986, La Clinica terapeutica,
Copied contents to your clipboard!