Sibship with histidinemia and an unrelated encephalopathy. Clinical and biochemical studies

Helv Paediatr Acta. 1977 Nov;32(4-5):401-11.

Abstract

Histidinemia was found in 3 of 4 siblings in one family, while a fatal encephalopathy with mental retardation was present in two of them and in the fourth child who did not have histidinemia. Biochemical studies of the histidinemic subjects showed elevated histidine levels in urine, CSF, and brain, while in a few urine samples histidine related imidazole compounds were found. Plasma levels of other amino acids were positively correlated with plasma histidine levels. Obesity and heart abnormalities appeared to be associated with the encephalopathy, which is probably of a new type. The histidinemia appears to be unrelated to the mental retardation or the encephalopathy in this family.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Amino Acid Metabolism, Inborn Errors / genetics*
  • Amino Acids / blood
  • Brain / metabolism
  • Brain Diseases / genetics*
  • Brain Diseases / metabolism
  • Child
  • Child, Preschool
  • Female
  • Heart Defects, Congenital / genetics
  • Histidine / blood*
  • Histidine / cerebrospinal fluid
  • Histidine / urine
  • Humans
  • Imidazoles / urine
  • Infant
  • Infant, Newborn
  • Intellectual Disability / genetics
  • Intellectual Disability / metabolism
  • Male
  • Obesity / genetics

Substances

  • Amino Acids
  • Imidazoles
  • Histidine