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A Chinese Classic Phenylketonuria Manifested as Autism

Published online by Cambridge University Press:  02 January 2018

C. H. Chen*
Affiliation:
Department of Psychiatry
K. J. Hsiao
Affiliation:
Clinical Biochemistry Research Laboratory, Department of Medical Research, Veterans' General Hospital, Taipei, Taiwan 11217, Republic of China
*
Peitou PO Box 2-207, Taipei, Taiwan 11216, Republic of China

Abstract

A 12-year-old Chinese boy had a diagnosis of infantile autism at infancy that was finally confirmed as classic phenylketonuria at adolescence. This treatable inborn metabolic disease should be investigated in cases of apparent autism, especially where mass neonatal screening of inborn metabolic diseases has not been established.

Type
Brief Reports
Copyright
Copyright © Royal College of Psychiatrists, 1989 

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