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Results 1 - 6 of 6 for Infantile liver failure syndrome 1
  1. MPV17-related hepatocerebral mitochondrial DNA depletion syndrome 
    ... in the liver and brain lead to the liver failure and neurological dysfunction associated with MPV17-related hepatocerebral mitochondrial DNA depletion syndrome. Researchers suggest that the less mtDNA that is ...
    https://medlineplus.gov/...bral-mitochondrial-dna-depletion-syndrome - Genetics
  2. Trichohepatoenteric syndrome 
    ... threatening in childhood, particularly in children who develop liver disease or severe infections. Trichohepatoenteric syndrome is a rare condition with an estimated prevalence of about 1 in 1 million people. At least 44 cases ...
    https://medlineplus.gov/.../condition/trichohepatoenteric-syndrome - Genetics
  3. Nephronophthisis 
    ... end-stage renal disease (ESRD), a life-threatening failure of kidney function ... around age 1 (infantile), around age 13 (juvenile), and around age 19 ( ...
    https://medlineplus.gov/genetics/condition/nephronophthisis - Genetics
  4. Cytochrome c oxidase deficiency 
    ... an enlarged liver (hepatomegaly), which may lead to liver failure. Most ... known as Leigh syndrome. The signs and symptoms of Leigh syndrome include ...
    https://medlineplus.gov/.../cytochrome-c-oxidase-deficiency - Genetics
  5. MEGDEL syndrome 
    ... Manov I, Saada A, Sprecher E, Mandel H. Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3-methylglutaconic aciduria type IV with sensorineural deafness, ...
    https://medlineplus.gov/genetics/condition/megdel-syndrome - Genetics
  6. Galactosialidosis 
    ... J, Ryan G, Velsher L, Chitayat D. Early-infantile galactosialidosis: prenatal presentation and postnatal follow-up. Am J Med Genet. 1999 Jul 2;85(1):38-47. Citation on PubMed Slama T, Garbade ...
    https://medlineplus.gov/genetics/condition/galactosialidosis - Genetics