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Results 1 - 8 of 8 for Acute liver failure
  1. Dihydrolipoamide dehydrogenase deficiency 
    ... dehydrogenase deficiency: a still overlooked cause of recurrent acute liver failure and Reye-like syndrome. Mol Genet Metab. 2013 ...
    https://medlineplus.gov/...dihydrolipoamide-dehydrogenase-deficiency - Genetics
  2. CPT1A gene 
    ... with abdominal pain and can rapidly progress to liver failure. Signs of acute fatty liver of pregnancy include an abnormal accumulation of fat ...
    https://medlineplus.gov/genetics/gene/cpt1a - Genetics
  3. HADHB gene 
    ... two serious liver disorders during pregnancy, known as acute fatty liver of pregnancy (AFLP) and HELLP syndrome. AFLP begins with abdominal pain and can rapidly progress to liver failure. HELLP stands for hemolysis (the breakdown of red ...
    https://medlineplus.gov/genetics/gene/hadhb - Genetics
  4. HADHA gene 
    ... two serious liver disorders during pregnancy, known as acute fatty liver of pregnancy (AFLP) and HELLP syndrome. AFLP begins with abdominal pain and can rapidly progress to liver failure. HELLP stands for hemolysis (the breakdown of red ...
    https://medlineplus.gov/genetics/gene/hadha - Genetics
  5. GATA1 gene 
    ... hepatomegaly), a buildup of scar tissue in the liver (hepatic fibrosis), ... acute megakaryoblastic leukemia (AMKL). The somatic GATA1 gene mutations ...
    https://medlineplus.gov/genetics/gene/gata1 - Genetics
  6. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency 
    ... 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy. Proc Natl Acad Sci U S ...
    https://medlineplus.gov/...-hydroxyacyl-coa-dehydrogenase-deficiency - Genetics
  7. Shwachman-Diamond syndrome 
    ... a cancer of blood-forming tissue known as acute myeloid leukemia (AML).Shwachman-Diamond syndrome also affects ... with Shwachman-Diamond syndrome and myelodysplastic syndrome or acute myeloid leukaemia: a multicentre, retrospective, cohort study. Lancet ...
    https://medlineplus.gov/.../condition/shwachman-diamond-syndrome - Genetics
  8. SAA1 gene 
    ... Whitehead AS. Tissue-specific regulation of the human acute-phase serum amyloid A genes, SAA1 and SAA2, ...
    https://medlineplus.gov/genetics/gene/saa1 - Genetics