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Jaundice and liver pigmentation syndrome in children
Dubin-Johnson syndrome is a disease characterized by intermittent jaundice. It is an autosomal dominant genetic disease with a clear family history. It is also called Dubin-Johnson syndrome, Dubin-Sprinz syndrome, Sprinz-Nelson syndrome, congenital non-hemolytic jaundice, congenital non-hemolytic jaundice type I, congenital non-hemolytic jaundice with increased direct bilirubin type I, black liver jaundice syndrome, etc.
  • Site of disease:

    Liver Skin
  • Infectious :

    Not contagious
  • Frequent population:

    baby
  • Related symptoms:

    Increased bilirubin Hepatomegaly Newborn jaundice after breastfeeding Loss of appetite Right upper abdominal pain
  • Concurrent disease:

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