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Urinary Alanine Excretor in a Huntington's Chorea Family

Published online by Cambridge University Press:  08 February 2018

Valerie Cowie  and
J. W. T. Seakins
Valerie Cowie
Affiliation:
Medical Research Council Psychiatric Genetics Research Unit, Maudsley Hospital, London, S.E.5
J. W. T. Seakins
Affiliation:
Hospital for Sick Children, Great Ormond Street, London, W.C.1
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Extract

In the course of urine-testing with Phenistix in a survey∗ of the inmates of remand homes, classifying schools and approved schools, only one positive result has been obtained from 2,300 boys and 541 girls tested so far in the London area. This was obtained with the urine of a boy who proved not to be Phenylketonuric, and further investigations were carried out in his case and with members of his family.

Information

Type
Clinical
Information
Journal of Mental Science , Volume 108 , Issue 455 , July 1962 , pp. 427 - 431
Copyright
Copyright © Royal College of Psychiatrists, 1962 

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References

Bell, J., “Huntington's Chorea”, Treas. hum. Inker., 1934, 4, part 1.Google Scholar
Bloxham, H. R., Day, M. G., Gibbs, N. K., and Woolf, L. I., “An Inborn Defect in the Metabolism of Tyrosine in Infants on a Normal Diet”, Biochem. J., 1960, 77, 320.CrossRefGoogle Scholar
Davenport, C. D., Huntington's Chorea in Relation to Heredity and Eugenics, 1916. Cold Spring Harbor, Long Island, N.Y. Google Scholar
Ghadimi, H., Partington, M. W., and Hunter, A., “A Familial Disturbance of Histidine Metabolism”, New Engl. J. Med., 1961, 265, 221.CrossRefGoogle Scholar
Mayer-Gross, W., Slater, E., and Roth, M., Clinical Psychiatry, 1960. London.Google Scholar
Menkes, J. H., and Jervis, G. A., “Development Retardation associated with an Abnormality in Tyrosine Metabolism”, Pediatrics, 1961, 28, 399.CrossRefGoogle Scholar
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