Síndrome de Bardet Biedl: rara causa de enfermedad renal terminal

Síndrome de Bardet Biedl: rara causa de enfermedad renal terminal

Bardet Biedl syndrome (SBB) is a rare genetic disorder; its prevalence in North America and Europe is estimated at 1: 140,000 to 1: 160,000 newborns. It is included in the group of ciliopathies as it results from at least 16 different gene mutations suspected of playing a fundamental role in the cil...

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Bibliographic Details
Main Author: Quinchuela Hidalgo, Jorge Oswaldo (author)
Other Authors: Nájera, Mercedes (author), Calispa, Franklin (author), Alcocer, Oswaldo (author), Chonata, Jorge (author)
Format: article
Language:spa
Published: 2016
Subjects:
síndrome de Bardet Biedl
ciliopatías
enfermedad renal crónica
hemodiálisis
Bardet Biedl syndrome
ciliopathies
chronic kidney disease
hemodialysis
Online Access:https://revistadigital.uce.edu.ec/index.php/CIENCIAS_MEDICAS/article/view/2853
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https://revistadigital.uce.edu.ec/index.php/CIENCIAS_MEDICAS/article/view/2853

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