Variabilidad genética y rol de los fenotipos oculares en el Síndrome de Stickler

Variabilidad genética y rol de los fenotipos oculares en el Síndrome de Stickler

Introducción: El Síndrome de Stickler (SS) es una anomalía del tejido conectivo que se caracteriza por alteraciones oculares, orofaciales, auditivas y esqueléticas. Aunque existen cuatro tipos de SS, la mayoría de las formas clínicas presentan alteraciones oculares como alta miopía, degeneración vit...

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Bibliographic Details
Main Authors:	Gretta Pantaleon Florido, Tamara Juvier Riesgo
Format:	Article
Language:	English
Published:	Universidad El Bosque 2021-11-01
Series:	Revista Salud Bosque
Subjects:	Síndrome de Stickler, fenotipo vítreo, COL2A1, COL11A1, COL9A1, COL9A2, Oftalmoartropatía.
Online Access:	https://revistas.unbosque.edu.co/index.php/RSB/article/view/3641

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