A Rare De Novo Robertsonian Translocation t(21q; 21q) in an Iranian Child With Down Syndrome: A Case Report

A Rare De Novo Robertsonian Translocation t(21q; 21q) in an Iranian Child With Down Syndrome: A Case Report

Down syndrome or trisomy 21 is the most common genetic disorder with a prevalence of 1 in 700 live-born infants. It is characterized by the intellectual disability of varying range, developmental delay, distinctive facial features and various physical abnormalities. The most frequent clinical featu...

Full description

Bibliographic Details
Main Authors: Ali Nikfar, Mojdeh Mansouri, Gita Fatemi Abhari
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2020-02-01
Series:Acta Medica Iranica
Subjects:
Down syndrome
Intellectual disability
Mental retardation
Robertsonian translocation
De novo
t21q: 21q
Online Access:https://acta.tums.ac.ir/index.php/acta/article/view/8050

Internet

https://acta.tums.ac.ir/index.php/acta/article/view/8050

Similar Items