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Oct 1, 2016 · M04.1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2024 edition of ICD-10-CM M04.1 became effective on October 1, 2023. This is the American ICD-10-CM version of M04.1 - other international versions of ICD-10 M04.1 may differ.
Nov 11, 2021 · Familial Mediterranean fever (FMF) is an inherited disorder that usually occurs in people of Mediterranean origin — including those of Jewish, Arab, Armenian, Turkish, North African, Greek or Italian ancestry. But it can affect people in any ethnic group. FMF is typically diagnosed during childhood.
Familial Mediterranean fever (FMF) is a hereditary inflammatory disorder. [1]: 149 FMF is an autoinflammatory disease caused by mutations in Mediterranean fever gene, which encodes a 781–amino acid protein called pyrin. [2]
Familial mediterranean fever. Familial non-neuropathic amyloidosis. Nonneuropathic heredofamilial amyloidosis. Clinical Information. 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.
Feb 1, 2024 · Familial Mediterranean fever (FMF) is characterized by recurrent attacks of fever and serositis (eg, peritonitis, pleuritis, pericarditis, synovitis) or erysipelas-like erythema. Most patients with FMF experience their first attack in early childhood.
Familial Mediterranean fever (FMF) is an autoinflammatory disorder characterized by recurrent short episodes of fever and serositis resulting in pain in the abdomen, chest, joints and muscles. ORPHA:342. Classification level: Disorder. Synonym (s): Benign paroxysmal peritonitis. Benign recurrent polyserositis. FMF. Familial paroxysmal polyserositis
Nov 11, 2021 · If you have signs and symptoms of familial Mediterranean fever, you may begin by seeing your family health care provider. Your health care provider may refer you to a specialist in inflammatory diseases (rheumatologist).
Familial Mediterranean fever is an inherited autoinflammatory syndrome characterised by recurrent short episodes of high fever associated with abdominal pain, inflammation of joints and other body sites and skin rash. If untreated, amyloidosis commonly develops and may have a fatal outcome.
Familial Mediterranean fever (FMF) is caused by an autosomal recessive mutation in the MEFV gene, which encodes the pyrin protein that helps modulate the inflammatory response in neutrophils. People with genetic origins in the Mediterranean basin are more commonly (but not exclusively) affected.
Aug 31, 2022 · Familial Mediterranean fever is primarily a genetic disease due to Mendelian-recessive inheritance of Mediterranean fever gene mutations. Occurs mainly in people of Mediterranean ancestry, especially from Arab countries, Turkey, Israel, and Armenia.
