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[An infant with hereditary methemoglobinemia]
L K Golterman1, P D Maaswinkel-Mooy
1Afd. Kindergeneeskunde, Academisch Ziekenhuis Leiden.
Abstract:
Autosomal recessive hereditary methemoglobinemia associated with mental retardation is a rare syndrome caused by a deficiency of the enzyme NADH cytochrome b5 reductase. A patient suffering from this disorder is described. The etiology of the syndrome and the (im)possibilities of treatment and prenatal diagnosis are discussed.