Literature DB >> 7551962

Autism, mental retardation, multiple exostoses and short stature in a female with 46,X,t(X;8)(p22.13;q22.1).

P Bolton1, J Powell, M Rutter, V Buckle, J R Yates, Y Ishikawa-Brush, A P Monaco.   

Abstract

A young adult female with multiple exostoses, short stature, autism, mental retardation and 46,X,t(X;8)(p22.13;q22.1) is described. Although the clinical features and translocation breakpoints raise the possibility of a number of specific conditions, the constellation of problems is not consistent with any previously reported genetic syndrome. It is argued that her clinical disorder is likely due to the chromosomal abnormality and that further detailed molecular genetic investigation may shed light on the genetic basis to various components of her phenotype including the autism.

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Year:  1995        PMID: 7551962     DOI: 10.1097/00041444-199522000-00001

Source DB:  PubMed          Journal:  Psychiatr Genet        ISSN: 0955-8829            Impact factor:   2.458


  5 in total

1.  Clinical Outcomes and Counselling Issues regarding Partial Trisomy of Terminal Xp in a Child with Developmental Delay.

Authors:  Karen L Sheath; Roberto L Mazzaschi; Salim Aftimos; Nerine E Gregersen; Alice M George; Donald R Love
Journal:  Sultan Qaboos Univ Med J       Date:  2013-05-09

Review 2.  Chromosomal disorders and autism.

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

3.  Autism-like socio-communicative deficits and stereotypies in mice lacking heparan sulfate.

Authors:  Fumitoshi Irie; Hedieh Badie-Mahdavi; Yu Yamaguchi
Journal:  Proc Natl Acad Sci U S A       Date:  2012-03-12       Impact factor: 11.205

4.  Systematic genotype-phenotype analysis of autism susceptibility loci implicates additional symptoms to co-occur with autism.

Authors:  Jacobine E Buizer-Voskamp; Lude Franke; Wouter G Staal; Emma van Daalen; Chantal Kemner; Roel A Ophoff; Jacob As Vorstman; Herman van Engeland; Cisca Wijmenga
Journal:  Eur J Hum Genet       Date:  2009-11-25       Impact factor: 4.246

5.  Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder.

Authors:  Kavita S Reddy
Journal:  BMC Med Genet       Date:  2005-01-18       Impact factor: 2.103

  5 in total

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