Literature DB >> 2297426

Cytogenetic survey for autistic fragile X carriers in a mental retardation center.

E S Cantú1, J W Stone, A A Wing, H R Langee, C A Williams.   

Abstract

A cytogenetic survey of 67 individuals previously identified as having mental retardation and autistic behaviors revealed 1 person (1.5%) with the fragile X chromosome (fra[X]) and 3 (4.5%) with autosome abnormalities. This low prevalence of fra(X) indicates that most persons with fra(X) in this mental retardation center did not have autistic behaviors severe enough to be identified as a secondary psychiatric diagnosis. The presence of other chromosomal abnormalities is consistent with the known causal heterogeneity of autism in mental retardation populations.

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Year:  1990        PMID: 2297426

Source DB:  PubMed          Journal:  Am J Ment Retard        ISSN: 0895-8017


  6 in total

Review 1.  Chromosomal disorders and autism.

Authors:  C Gillberg
Journal:  J Autism Dev Disord       Date:  1998-10

2.  Molecular and cytogenetic analyses on Brazilian youths with pervasive developmental disorders.

Authors:  MarcosRobertoHigino Estécio; Agnes Cristina Fett-Conte; Marileila Varella-Garcia; Cíntia Fridman; Ana Elizabete Silva
Journal:  J Autism Dev Disord       Date:  2002-02

3.  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

4.  The HOPA gene dodecamer duplication is not a significant etiological factor in autism.

Authors:  R C Michaelis; S A Copeland-Yates; K Sossey-Alaoui; C Skinner; M J Friez; J W Longshore; R J Simensen; R J Schroer; R E Stevenson
Journal:  J Autism Dev Disord       Date:  2000-08

5.  Autistic features in children with mental retardation.

Authors:  N Kar; R Khanna; G C Kar
Journal:  Indian J Psychiatry       Date:  1997-10       Impact factor: 1.759

6.  The genetic overlap of attention deficit hyperactivity disorder and autistic spectrum disorder.

Authors:  Arie J Stam; Patricia F Schothorst; Jacob As Vorstman; Wouter G Staal
Journal:  Appl Clin Genet       Date:  2009-03-10
  6 in total

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