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・ Familial British dementia
・ Familial cirrhosis
・ Familial dysalbuminemic hyperthyroxinemia
・ Familial dysautonomia
・ Familial dysbetalipoproteinemia
・ Familial encephalopathy with neuroserpin inclusion bodies
・ Familial exudative vitreoretinopathy
・ Familial hemiplegic migraine
・ Familial homicide
・ Familial hyperaldosteronism
・ Familial hypercholesterolemia
・ Familial hypertriglyceridemia
・ Familial hypocalciuric hypercalcemia
・ Familial isolated vitamin E deficiency
・ Familial male-limited precocious puberty
Familial Mediterranean fever
・ Familial multiple intestinal atresia
・ Familial myxovascular fibromas
・ Familial partial lipodystrophy
・ Familial progressive hyperpigmentation
・ Familial renal amyloidosis
・ Familial renal disease in animals
・ Familial thoracic aortic aneurysm
・ Familialism
・ Familianten
・ Familiar (disambiguation)
・ Familiar (Dungeons & Dragons)
・ Familiar bluet
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Familial Mediterranean fever : ウィキペディア英語版
Familial Mediterranean fever

Familial Mediterranean fever (FMF), also known as Armenian disease, is a hereditary inflammatory disorder.〔James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. ISBN 0-7216-2921-0.〕 FMF is an autoinflammatory disease caused by mutations in MEFV, a gene which encodes a 781–amino acid protein denoted pyrin.
The disorder has been given various names including familial paroxysmal polyserositis, periodic peritonitis, recurrent polyserositis, benign paroxysmal peritonitis, periodic disease or periodic fever, Reimann periodic disease or Reimann's syndrome, Siegal-Cattan-Mamou disease, and Wolff periodic disease. Note that "periodic fever" can also refer to any of the Periodic fever syndromes.
==Signs and symptoms==


抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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