Chronic familial Mediterranean fever with development of secondary amyloidosis.

A 20-year-old Turkish male presented with fever, abdominal pain, and systemic lethargy. His clinical history revealed symptoms to be self-limiting but reoccuring over the past six months. Blood and urine specimens collected indicated amyloidosis. A kidney CT image indicated kidney inflammation. He w...

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Publicado en:Clinical Laboratory Science Vol. 24; no. 1; pp. 2 - 8
Autor principal: Larrimore, Christopher
Formato: tables/charts Journal Article
Publicado: American Society for Clinical Laboratory Science Winter2011
Acceso en línea:Ver este registro en EBSCOhost
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      pub: American Society for Clinical Laboratory Science
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        atl: Chronic familial Mediterranean fever with development of secondary amyloidosis.
      aug:
        au: Larrimore, Christopher
      sug:
        subj:
          Amyloidosis, Secondary
          Hereditary Diseases
          Inflammation Familial and Genetic
          Blood Cell Count
          Colchicine Therapeutic Use
          Genes
          Hereditary Diseases Diagnosis
          Hereditary Diseases Drug Therapy
          Hereditary Diseases Physiopathology
          Hereditary Diseases Symptoms
          Inflammation Drug Therapy
          Inflammation Physiopathology
          Urinalysis
      ab: A 20-year-old Turkish male presented with fever, abdominal pain, and systemic lethargy. His clinical history revealed symptoms to be self-limiting but reoccuring over the past six months. Blood and urine specimens collected indicated amyloidosis. A kidney CT image indicated kidney inflammation. He was diagnosed with Familial Mediterranean Fever with the development of secondary amyloidosis and treated with colchicine.
      pubtype: Academic Journal
      doctype:
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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