Detection of the I172N Mutation in Cuban Patients with Congenital Adrenal Hyperplasia due to 21 Hydroxylase Insufficiency

Detection of the I172N Mutation in Cuban Patients with Congenital Adrenal Hyperplasia due to 21 Hydroxylase Insufficiency

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<strong>Background:</strong> congenital adrenal hyperplasia is the most frequent cause of sexual ambiguity in childhood. Molecular diagnosis is an element to be considered for the management and genetic counseling of patients and relatives at risk. <br /><strong>Objective:<...

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Bibliographic Details
Main Authors: Taimí Barrueta Ordóñez, Teresa Collazo Mesa, Paulina Lantigua Cruz, Adrián de Jesús González Navarro, Tania Espinosa Reyes
Format: Article
Language:Spanish
Published: Universidad de las Ciencias Médicas de Cienfuegos 2019-02-01
Series:Revista Finlay
Subjects:
hiperplasia suprarrenal congénita
análisis mutacional de adn
patología molecular
estudios transversales
cuba
Online Access:http://www.revfinlay.sld.cu/index.php/finlay/article/view/685

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http://www.revfinlay.sld.cu/index.php/finlay/article/view/685

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