Literature DB >> 2597924

A Chinese classic phenylketonuria manifested as autism.

C H Chen1, K J Hsiao.   

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.

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Year:  1989        PMID： 2597924     DOI： 10.1192/bjp.155.2.251

Source DB:  PubMed          Journal:  Br J Psychiatry        ISSN： 0007-1250            Impact factor:   9.319


  2 in total

1.  Clinical review: Medical differential diagnosis and treatment of the autistic syndrome.

Authors:  Mary Coleman
Journal:  Eur Child Adolesc Psychiatry       Date:  1993-07       Impact factor: 4.785

2.  Clinical and neuropsychological outcomes for children with phenylketonuria in Upper Egypt; a single-center study over 5 years.

Authors:  Abdelrahim A Sadek; Mohammed H Hassan; Nesreen A Mohammed
Journal:  Neuropsychiatr Dis Treat       Date:  2018-10-05       Impact factor: 2.570
  2 in total

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