Recurrent polyserositis(familial mediterranean fever).
نویسندگان
چکیده
منابع مشابه
Patient with Recurrent Polyserositis (Familial Mediterranean Fever).
Familial Mediterranean fever (FMF) is a hereditary autosomal recessive ,systemic, auto-inflammatory disorder characterized by sporadic, unpredictable attacks of fever and serosal inflammation. FMF is caused by mutations in MEFV, a gene located on the short arm of chromosome 16 (16p13) which encodes a protein 'Pyrin'. The disorder has been given various names including familial paroxysmal polyse...
متن کاملrecurrent henoch-schönlein purpura in familial mediterranean fever
familial mediterranean fever (fmf) is a relatively rare disorder, characterized by recurrent self-limited attacks of fever and polyserositis. diagnosis is made by clinical features, gene identification on chromosome 16 and clinical response to specific treatment. different types of vasculitis have been reported in fmf. henoch-schönlein purpura (hsp) is one of them, usually with a benign clinica...
متن کاملIsolated recurrent pleuritis revealing familial mediterranean Fever in adulthood.
Familial Mediterranean fever (FMF) is a genetic autoinflammatory disease especially affecting populations of Mediterranean origin with an autosomal recessive inheritance. The cardinal manifestations consist of short febrile and painful attacks of peritonitis, arthritis and pleuritis developing during childhood. We report the case of a 26-year-old man of Tunisian descent who had febrile episodes...
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ژورنال
عنوان ژورنال: Japanese Journal of Medicine
سال: 1987
ISSN: 0021-5120,1881-123X
DOI: 10.2169/internalmedicine1962.26.370