Down Syndrome Resulting from a Rare non-Robertsonian Translocation t(11;21)(p13;q22)

Down Syndrome Resulting from a Rare non-Robertsonian Translocation t(11;21)(p13;q22)

Introduction: Down syndrome (DS) is a common genetic disorder, occurring in approximately 1 in 700 births. It results from an extra copy (triplication) of the whole or part of the long arm of chromosome 21 caused by different cytogenetic alterations: free trisomy, Robertsonian translocations, mosaic...

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Bibliographic Details
Main Authors: Dante Bruno Avanso Rosan, Priscila L. Dourado, Andréa Engracia Ruiz, Valéria C.C. Ferrarezi da Silva, Cristina Benitez Vendrame, Andréa B. Carvalho-Salles, Brasilina de F. Mafei, Agnes Cristina Fett -Conte
Format: Article
Language:Portuguese
Published: Faculdade de Medicina de São José do Rio Preto 2021-08-01
Series:Arquivos de Ciências da Saúde
Subjects:
Trisomy; Chromosomes, Human, Pair 11; Translocation, Genetic; Genetic counseling
Online Access:https://ahs.famerp.br/index.php/ahs/article/view/49

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https://ahs.famerp.br/index.php/ahs/article/view/49

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