Literature DB >> 6444857

A cytogenetic survey of 449 patients in a Japanese institution for the mentally retarded.

I Kondo, H Hamaguchi, S Nakajima, T Haneda.   

Abstract

A cytogenetic survey was carried out on 449 patients (261 males and 188 females) in an institution for the mentally retarded in Japan. A total of 37 patients (8.1%) were shown to have chromosome abnormalities. There were 33 individuals (7.3%) with 21 trisomy. In addition, we found one patient with 46,XY/47,XY,+12p, one with 46,XY,r(22), and one with 45,XY,-13,-14,+t(13q14q). Only one female was found to have an abnormal sex chromosome constitution, 47,XXX. The significant contribution of chromosome abnormalities in the etiology of mental retardation is also shown in the present survey. The most common chromosome abnormality was 21 trisomy, as seen in other similar surveys.

Entities:  

Mesh:

Year:  1980        PMID: 6444857     DOI: 10.1111/j.1399-0004.1980.tb00130.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  6 in total

1.  Chromosomal Microarray Detection of Constitutional Copy Number Variation Using Saliva DNA.

Authors:  Jennifer Reiner; Lisa Karger; Ninette Cohen; Lakshmi Mehta; Lisa Edelmann; Stuart A Scott
Journal:  J Mol Diagn       Date:  2017-03-18       Impact factor: 5.568

2.  Multifocal meningiomas in a patient with a constitutional ring chromosome 22.

Authors:  T Arinami; I Kondo; H Hamaguchi; S Nakajima
Journal:  J Med Genet       Date:  1986-04       Impact factor: 6.318

Review 3.  Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.

Authors:  David T Miller; Margaret P Adam; Swaroop Aradhya; Leslie G Biesecker; Arthur R Brothman; Nigel P Carter; Deanna M Church; John A Crolla; Evan E Eichler; Charles J Epstein; W Andrew Faucett; Lars Feuk; Jan M Friedman; Ada Hamosh; Laird Jackson; Erin B Kaminsky; Klaas Kok; Ian D Krantz; Robert M Kuhn; Charles Lee; James M Ostell; Carla Rosenberg; Stephen W Scherer; Nancy B Spinner; Dimitri J Stavropoulos; James H Tepperberg; Erik C Thorland; Joris R Vermeesch; Darrel J Waggoner; Michael S Watson; Christa Lese Martin; David H Ledbetter
Journal:  Am J Hum Genet       Date:  2010-05-14       Impact factor: 11.025

4.  Frequency of the fragile X syndrome in Japanese mentally retarded males.

Authors:  T Arinami; I Kondo; S Nakajima
Journal:  Hum Genet       Date:  1986-08       Impact factor: 4.132

5.  Ring chromosome 22: a review of the literature and first report from India.

Authors:  S Mahajan; A Kaur; J Singh
Journal:  Balkan J Med Genet       Date:  2012-06       Impact factor: 0.519

6.  Neuropsychiatric decompensation in adolescents and adults with Phelan-McDermid syndrome: a systematic review of the literature.

Authors:  Alexander Kolevzon; Elsa Delaby; Elizabeth Berry-Kravis; Joseph D Buxbaum; Catalina Betancur
Journal:  Mol Autism       Date:  2019-12-24       Impact factor: 7.509

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.