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Results 1 - 10 of 23 for Infantile liver failure
  1. Carnitine palmitoyltransferase II deficiency 
    ... such as viral infections. Individuals with the severe infantile hepatocardiomuscular form 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
  2. Hepatic hemangioma 
    ... ruptures, the only sign may be an enlarged liver. Babies with benign infantile hemangioendothelioma may have: A growth in the abdomen Anemia Signs of heart failure The following tests may be performed: Blood tests ...
    https://medlineplus.gov/ency/article/000243.htm - Medical Encyclopedia
  3. Pompe disease 
    ... onset, and late-onset.The classic form of infantile-onset Pompe disease begins ... rate (failure to thrive) and have breathing problems. If untreated, ...
    https://medlineplus.gov/genetics/condition/pompe-disease - Genetics
  4. 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
  5. 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
  6. 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 same features as the progressive hepatic type, but the liver disease is not as severe. In the non- ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-iv - Genetics
  7. Combined oxidative phosphorylation deficiency 1 
    ... oxidative phosphorylation deficiency 1, with individuals quickly developing liver failure. Individuals with this condition also usually have a ...
    https://medlineplus.gov/...ed-oxidative-phosphorylation-deficiency-1 - Genetics
  8. Cytochrome c oxidase deficiency 
    ... an enlarged liver (hepatomegaly), which may lead to liver failure. Most individuals with cytochrome c oxidase deficiency have ...
    https://medlineplus.gov/.../cytochrome-c-oxidase-deficiency - Genetics
  9. Lipid Storage Diseases From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Leukodystrophies/Specifics ... Leukodystrophies ... Genetic Brain Disorders/Specifics ... Genetic Brain Disorders ... Tay-Sachs Disease/Related Issues ... Tay-Sachs Disease ... Lipid ...
    https://www.ninds.nih.gov/.../disorders/lipid-storage-diseases - External Health Links
  10. Polycystic kidney disease 
    ... to become enlarged and can lead to kidney failure. Cysts may also develop in other organs, particularly the liver.Frequent complications of polycystic kidney disease include dangerously ...
    https://medlineplus.gov/genetics/condition/polycystic-kidney-disease - Genetics
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