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  2. Gilbert's syndrome - Wikipedia

    en.wikipedia.org/wiki/Gilbert's_syndrome

    Mild jaundice may appear under conditions of exertion, stress, fasting, and infections, but the condition is otherwise usually asymptomatic. [7] [8] Severe cases are seen by yellowing of the skin tone and yellowing of the conjunctiva in the eye. [9] Gilbert syndrome has been reported to contribute to an accelerated onset of neonatal jaundice.

  3. Liver disease - Wikipedia

    en.wikipedia.org/wiki/Liver_disease

    Hepatitis, inflammation of the liver, is caused by various viruses (viral hepatitis) also by some liver toxins (e.g. alcoholic hepatitis), autoimmunity (autoimmune hepatitis) or hereditary conditions. [6] Alcoholic liver disease is a hepatic manifestation of alcohol overconsumption, including fatty liver disease, alcoholic hepatitis, and ...

  4. Dubin–Johnson syndrome - Wikipedia

    en.wikipedia.org/wiki/Dubin–Johnson_syndrome

    Dubin–Johnson syndrome is a rare, autosomal recessive, benign disorder that causes an isolated increase of conjugated bilirubin in the serum. Classically, the condition causes a black liver due to the deposition of a pigment similar to melanin. [2]

  5. Wilson's disease - Wikipedia

    en.wikipedia.org/wiki/Wilson's_disease

    The condition is autosomal recessive; for people to be affected, they must inherit a mutated copy of the gene from both parents. Diagnosis may be difficult and often involves a combination of blood tests, urine tests, and a liver biopsy. Genetic testing may be used to screen family members of those affected. [1]

  6. Ornithine transcarbamylase deficiency - Wikipedia

    en.wikipedia.org/wiki/Ornithine_transcarbamylase...

    Genetic mutation. [1] Diagnostic method: Liver function tests, genetic testing, and a liver biopsy. [1] Differential diagnosis: urea cycle disorders, fulminant hepatitis, Citrin deficiency, and hyperornithinemia-hyperammonemia-homocitrullinuria syndrome. [2] Treatment: Hydration, arginine, and hemodialysis. [1] Prognosis: 50% of infants with ...

  7. Alagille syndrome - Wikipedia

    en.wikipedia.org/wiki/Alagille_syndrome

    Alagille syndrome (ALGS) is a genetic disorder that affects primarily the liver and the heart. Problems associated with the disorder generally become evident in infancy or early childhood. Problems associated with the disorder generally become evident in infancy or early childhood.