z-logo
open-access-imgOpen Access
Cytogenetic analysis in a large series of children with non-syndromic mental retardation
Author(s) -
Abir Gmidène,
Soumaya Mougou-Zrelli,
Hanene Hannachi,
Najla Soyah,
Naoufel Gadour,
Imed Harrabi,
Hatem Elghezal,
Saad Ali,
Inesse Ben Abdallah Bouhjar
Publication year - 2015
Publication title -
journal of pediatric genetics
Language(s) - English
Resource type - Journals
eISSN - 2146-4596
pISSN - 2146-460X
DOI - 10.3233/pge-2012-027
Subject(s) - etiology , medicine , pediatrics , cytogenetics , chromosomal analysis , congenital malformations , chromosome analysis , molecular cytogenetics , population , growth retardation , epilepsy , intellectual disability , karyotype , chromosome , psychiatry , genetics , biology , pregnancy , environmental health , gene
Mental retardation affects 1-3% of the population. To evaluate the implication of chromosomal abnormalities in the etiology of mental retardation, 1420 patients with non-syndromic mental retardation recruited at the department of cytogenetics of Farhat Hached hospital (Sousse, Tunisia) between January 2005 and December 2009, were analyzed using standard cytogenetic techniques. Age ranged between 3 and 18 years with a median of 8 years. Chromosomal abnormalities were detected in 7.8% of patients and an increased prevalence of chromosome anomalies was observed in patients when the mental retardation is associated with a severe degree of intellectual disability, facial dysmorphic features and/or congenital malformations or epilepsy.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom