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 featur...

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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

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