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Results 1 - 10 of 16 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. Citrullinemia 
    ... OR ADULT ONSET; CDAA CITRIN DEFICIENCY, NEONATAL OR INFANTILE ONSET; CDNI PubMed Faghfoury H, Baruteau J, de Baulny HO, Haberle J, Schulze A. Transient fulminant liver failure as an initial presentation in citrullinemia type I. ...
    https://medlineplus.gov/genetics/condition/citrullinemia - Genetics
  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. Galactosialidosis 
    ... and kidney disease that can progress to kidney failure. Infants with this form usually are diagnosed between birth and 3 months of age; they typically live to around 6 months of age.The late infantile form of galactosialidosis shares some features with the ...
    https://medlineplus.gov/genetics/condition/galactosialidosis - Genetics
  10. Niemann-Pick disease 
    ... Pick disease type A usually develop an enlarged liver and spleen (hepatosplenomegaly) by age 3 months and fail to gain weight and grow at the expected rate (failure to thrive). The affected children develop normally until ...
    https://medlineplus.gov/genetics/condition/niemann-pick-disease - Genetics
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