Verdu A, Lopez-Herce J, Pascual-Castroviejo I, Martinez-Bermejo A, Ugarte M, Garcia M J
Acta Paediatr Scand. 1985 Sep;74(5):815-8. doi: 10.1111/j.1651-2227.1985.tb10041.x.
A female infant with an intermediate variant of maple syrup urine disease is described. The patient had psychomotor retardation and high plasma levels of branched chain aminoacids. Leucine decarboxylation rate in leukocytes was diminished. Cranial computed tomography showed decreased density in the cerebral white matter. After starting dietary treatment the infant resumed her psychomotor development and the abnormal images previously seen on computed tomography disappeared.