Home > D. Systemic pathology > Genetic and developmental anomalies > Genetic metabolic diseases > defect in 25-hydroxylase
defect in 25-hydroxylase
Tuesday 26 May 2009
An inborn error in sterol 25-hydroxylase (CH25H), which is involved in the alternative pathway for bile acid side-chain synthesis, has been suggested to account for the bile acid profile that is found in some cases of neonatal hepatitis syndrome.
This is characterized by the presence of low levels of normal primary bile acids in serum and increased urinary excretion of typical bile alcohols.