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Article

18q- chromosomal abnormality in a phenotypically normal 2 1/2-year-old male with autism.

Developmental medicine and child neurology - 1 Nov 1992

Seshadri K, Wallerstein R, Burack G

Abstract excerpt

The authors report the case of a 2 1/2-year-old male with autism, with an 18q- chromosomal abnormality in the absence of phenotypical features of the 18q- syndrome. It is suggested that clinicians evaluating children with autistic disorders consider obtaining chromosome analysis, even in the absence of phenotypical abnormalities.

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Source

Identifiers

PMID: 1426678
DOI: 10.1111/j.1469-8749.1992.tb11406.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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