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Results 1 - 10 of 40 for Hepatic failure
  1. Progressive familial intrahepatic cholestasis 
    ... causes progressive liver disease, which typically leads to liver failure. In people with PFIC, liver cells are less ... K) in the blood. Affected individuals typically develop liver failure before adulthood.The signs and symptoms of PFIC2 ...
    https://medlineplus.gov/...ressive-familial-intrahepatic-cholestasis - Genetics
  2. MPV17-related hepatocerebral mitochondrial DNA depletion syndrome 
    ... infants develop liver disease that quickly progresses to liver failure. The liver is frequently enlarged (hepatomegaly) and liver ... in the liver and brain lead to the liver failure and neurological dysfunction associated with MPV17-related hepatocerebral ...
    https://medlineplus.gov/...bral-mitochondrial-dna-depletion-syndrome - Genetics
  3. Deoxyguanosine kinase deficiency 
    ... signs of liver disease which may result in liver failure. They also develop progressive neurological problems including very ... viral infection predispose apparently healthy children to fulminant liver failure. J Pediatr Gastroenterol Nutr. 2009 Jul;49(1): ...
    https://medlineplus.gov/.../deoxyguanosine-kinase-deficiency - Genetics
  4. MPV17 gene 
    ... in the liver and brain lead to the liver failure and neurological dysfunction associated with MPV17-related hepatocerebral ... the MPV17 gene are responsible for rapidly progressive liver failure in infancy. Hepatology. 2007 Oct;46(4):1218- ...
    https://medlineplus.gov/genetics/gene/mpv17 - Genetics
  5. Dihydrolipoamide dehydrogenase deficiency 
    ... from an enlarged liver (hepatomegaly) to life-threatening liver failure. In some affected people, liver disease, which can ... 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
  6. Carnitine palmitoyltransferase II deficiency 
    ... form of the disorder develop respiratory failure, seizures, liver failure, a weakened heart muscle (cardiomyopathy), and an irregular ... of CPT II deficiency are at risk for liver failure, nervous system damage, coma, and sudden death.The ...
    https://medlineplus.gov/...nitine-palmitoyltransferase-ii-deficiency - Genetics
  7. Mitochondrial complex III deficiency 
    ... such as liver disease that can lead to liver failure, kidney abnormalities (tubulopathy), and brain dysfunction (encephalopathy). Encephalopathy ... III deficiency in patients with tubulopathy, encephalopathy and liver failure. Nat Genet. 2001 Sep;29(1):57-60. ...
    https://medlineplus.gov/.../mitochondrial-complex-iii-deficiency - Genetics
  8. Glycogen storage disease type IV 
    ... hepatic type of GSD IV often die of liver failure in early childhood.The non-progressive hepatic type of GSD IV has many of the ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-iv - Genetics
  9. Hepatic veno-occlusive disease with immunodeficiency 
    ... a buildup of scar tissue (hepatic fibrosis), and liver failure.Children with VODI are prone to recurrent infections caused by certain bacteria, viruses, and fungi. The organisms that cause ... before hepatic veno-occlusive disease becomes evident.Many people with ...
    https://medlineplus.gov/...o-occlusive-disease-with-immunodeficiency - Genetics
  10. 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 in the liver, hypoglycemia, increased levels of ammonia in the blood (hyperammonemia), ... M, Girard J, Prip-Buus C. Modulation of the hepatic malonyl-CoA-carnitine palmitoyltransferase 1A partnership creates a ...
    https://medlineplus.gov/genetics/gene/cpt1a - Genetics
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