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Phenylketonuria

A review and a report of the pathological findings in four cases

Published online by Cambridge University Press:  08 February 2018

L. Crome and
C. M. B. Pare
L. Crome
Affiliation:
Fountain Hospital, and the Bethlem Royal and the Maudsley Hospital London
C. M. B. Pare
Affiliation:
Fountain Hospital, and the Bethlem Royal and the Maudsley Hospital London
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Phenylketonuria is an inborn error of metabolism characterized by excretion of phenylpyruvic acid in the urine and usually by severe mental defect and certain bodily features of which dilution of pigment is the most noticeable.

Information

Type
Original Articles
Information
Journal of Mental Science , Volume 106 , Issue 444 , July 1960, pp. 862 - 883
Copyright
Copyright © Royal College of Psychiatrists, 1960 

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