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Results 1 - 10 of 10 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 
    ... develop in women during pregnancy. This disorder, called acute fatty liver of pregnancy (AFLP), begins with abdominal pain and can rapidly progress to liver failure. Signs of AFLP include an abnormal accumulation of ...
    https://medlineplus.gov/genetics/gene/cpt1a - Genetics
  3. Carnitine palmitoyltransferase I deficiency 
    ... are at risk of developing a condition called acute fatty liver of pregnancy (AFLP). AFLP begins with abdominal pain and can rapidly progress to liver failure. Carnitine palmitoyltransferase IA deficiency CPT 1A deficiency CPT ...
    https://medlineplus.gov/...rnitine-palmitoyltransferase-i-deficiency - 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. 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
  6. 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
  7. 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
  8. Fanconi anemia 
    ... developing a cancer of blood-forming cells called acute myeloid leukemia (AML). They are also at risk of developing tumors of the liver, gastrointestinal system, genital tract, or head and neck ( ...
    https://medlineplus.gov/genetics/condition/fanconi-anemia - Genetics
  9. 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
  10. 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