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Results 1 - 9 of 9 for Infantile liver failure syndrome 3
  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. 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, encephalopathy ...
    https://medlineplus.gov/genetics/condition/megdel-syndrome - Genetics
  3. MPV17 gene 
    ... 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/genetics/gene/mpv17 - Genetics
  4. 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
  5. Lipid Storage Diseases From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Lipid storage diseases (also known as lipidoses) are a group of inherited metabolic disorders in which harmful amounts of fatty materials (lipids) accumulate ...
    https://www.ninds.nih.gov/.../disorders/lipid-storage-diseases - External Health Links
  6. 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
  7. Trichohepatoenteric syndrome 
    ... trichorrhexis nodosa.Other signs and symptoms of trichohepatoenteric syndrome can include liver disease; skin abnormalities; and distinctive facial features, including ...
    https://medlineplus.gov/.../condition/trichohepatoenteric-syndrome - Genetics
  8. Nephronophthisis 
    ... with nephronophthisis have additional features, which can include liver fibrosis, heart abnormalities, or mirror image reversal of the position of one or more organs inside the body (situs inversus).Nephronophthisis can occur as part of separate syndromes that affect other areas of the body; these ...
    https://medlineplus.gov/genetics/condition/nephronophthisis - Genetics
  9. Corticotropin, Repository Injection 
    ... When corticotropin repository injection is used to treat infantile spasms, it ... once a day for 2 to 3 weeks, and then the dose is gradually decreased. ...
    https://medlineplus.gov/druginfo/meds/a613006.html - Drugs and Supplements