Affiliations 

  • 1 Puleri Jamilalul Noor, BSc Hons (Mal). Research Officer (Geneticist), Department of Haematology Institute for Medical Research, Jalan Pahang, 50588 Kuala Lumpur, Malaysia.
  • 2 Y M Chin, BSc Hons (Mal). Research Officer (Genelicist). Department of Haematology, Institute for Medical Research, Jalan Pahang, 50588 Kuala Lumpur, Malaysia.
  • 3 S K Ten, BSc Hons (Mal), MSc (Mal). Research Officer (Geneticist), Department of Haematology, Institute for Medical Research, Jalan Pahang, 50588 Kuala Lumpur, Malaysia.
  • 4 Khalid Hassan, MBBS (S'pore), MRCP (UK), MRCPath, DCP (Lond), DTM & H (B'kok). Head, Department of Haematology, Institute for Medical Research, Jalan Pahang, 50588 Kuala Lumpur, Malaysia.
Singapore Med J, 1987 Jun;28(3):235-40.
PMID: 2958941

Abstract

A cytogenetic survey 01 124 children in lour special schools for the mentally handicapped was carried out to determine the contribution of chromosomal abnormalities to the aetiology of mental retardation in these children. All the children were karyotyped employing the G·banding technique 01 43 (34.7%) with an abnormal chromosome complement, 40 had Down's Syndrome, and 3 had other chromosomal abnormalities, namely a translocation 1;17, a mosaic male/trisomy 18 and a Klinefelter's syndrome. Polymorphic variants involving chromosomes 1, 9, and 14 were also observed. Two other children showed variants of the Y chromosome (one a small Y and the other a metacentric Y). The possible contribution by these abnormal variants to mental retardation is discussed. Details of the abnormal cytogenetic findings are reported.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.