Inborn errors of metabolism: Clues to understanding human behavioral disorders
- 1 July 1976
- journal article
- research article
- Published by Springer Nature in Behavior Genetics
- Vol. 6 (3), 263-284
- https://doi.org/10.1007/bf01065723
Abstract
Detailed behavioral and biochemical investigation of patients with inborn errors of metabolism, especially those intrinsic to the nervous system, may provide many clues to the genetic predisposition underlying human behavioral traits. Relatives of such patients and other individuals with homologous enzymatic lesions due to alleles specifying intermediate activity need to be studied as well. Among the metabolic disorders discussed selectively here, some masquerade as schizophrenia, manic-depressive illness, or hyperactivity syndrome of childhood, providing examples of the striking heterogeneity to be found for these common behavioral disorders.This publication has 39 references indexed in Scilit:
- NEW VARIANT OF PHENYLKETONURIA WITH PROGRESSIVE NEUROLOGICAL ILLNESS UNRESPONSIVE TO PHENYLALANINE RESTRICTIONThe Lancet, 1975
- Congenital adrenal hyperplasia. II. Cognitive and behavioral studiesBehavior Genetics, 1975
- Congenital adrenal hyperplasia. I. Family studies of IQBehavior Genetics, 1975
- Correlation of erythrocyte catechol-O-methyltransferase activity between siblingsNature, 1974
- Two functional X chromosomes in human fetal oocytesExperimental Cell Research, 1973
- Dopamine-β-Hydroxylase Deficits in the Brains of Schizophrenic PatientsScience, 1973
- FAMILY HISTORY AND HALF‐SIBLING RESEARCH IN ALCOHOLISM*Annals of the New York Academy of Sciences, 1972
- Reduced Catechol- O -Methyltransferase Activity in Red Blood Cells of Women with Primary Affective DisorderScience, 1970
- Intelligence quotients and intelligence loss in patients with phenylketonuria and some variant statesThe Journal of Pediatrics, 1970
- MAPLE SYRUP URINE DISEASE METABOLITES STUDIED IN CEREBELLUM CULTURES1Journal of Neurochemistry, 1969