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A Chinese classic phenylketonuria manifested as autism.

作者信息

Chen C H, Hsiao K J

机构信息

Department of Psychiatry, Veterans' General Hospital, Taipei, Taiwan, Republic of China.

出版信息

Br J Psychiatry. 1989 Aug;155:251-3. doi: 10.1192/bjp.155.2.251.

DOI:10.1192/bjp.155.2.251
PMID:2597924
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.

摘要

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引用本文的文献

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Clinical and neuropsychological outcomes for children with phenylketonuria in Upper Egypt; a single-center study over 5 years.埃及上埃及地区苯丙酮尿症患儿的临床和神经心理学结局;一项为期5年的单中心研究
Neuropsychiatr Dis Treat. 2018 Oct 5;14:2551-2561. doi: 10.2147/NDT.S176198. eCollection 2018.
2
Clinical review: Medical differential diagnosis and treatment of the autistic syndrome.临床综述:自闭症谱系障碍的医学鉴别诊断与治疗
Eur Child Adolesc Psychiatry. 1993 Jul;2(3):161-168. doi: 10.1007/BF02125571.