Crigler-Najjar Syndrome

This rare inherited syndrome is characterized by a lack of glucuronyl. See also liver structure and function and assessment of patients with liver disease.) This rare inherited syndrome is characterized by a lack of glucuronyl. See also liver structure and function and assessment of patients with liver disease.) Patients with autosomal recessive type I disease (complete) have a severe hyperbilirubinemia. They usually die from the effects of kernicterus at the…

September 3, 2018
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