Please use this identifier to cite or link to this item:
Type: Artigo
Title: Glycogen storage diseases : twenty‐seven new variants in a cohort of 125 patients
Author: Sperb-Ludwig, Fernanda
Pinheiro, Franciele Cabral
Soares, Malu Bettio
Nalin, Tatiele
Ribeiro, Erlane Marques
Steiner, Carlos Eduardo
Valadares, Eugênia Ribeiro
Porta, Gilda
Souza, Carolina Fishinger Moura de
Schwartz, Ida Vanessa Doederlein
Abstract: Hepatic glycogen storage diseases (GSDs) are a group of rare genetic disorders in which glycogen cannot be metabolized to glucose in the liver because of enzyme deficiencies along the glycogenolytic pathway. GSDs are well‐recognized diseases that can occur without the full spectrum, and with overlapping in symptoms.We analyzed a cohort of 125 patients with suspected hepatic GSD through a next‐generation sequencing (NGS) gene panel in Ion Torrent platform. New variants were analyzed by pathogenicity prediction tools.Twenty‐seven new variants predicted as pathogenic were found between 63 variants identified. The most frequent GSD was type Ia (n = 53), followed by Ib (n = 23). The most frequent variants were p.Arg83Cys (39 alleles) and p.Gln347* (14 alleles) in G6PC gene, and p.Leu348Valfs (21 alleles) in SLC37A4 gene.The study presents the largest cohort ever analyzed in Brazilian patients with hepatic glycogenosis. We determined the clinical utility of NGS for diagnosis. The molecular diagnosis of hepatic GSDs enables the characterization of diseases with similar clinical symptoms, avoiding hepatic biopsy and having faster results.
Subject: Doença de depósito de glicogênio
Diagnóstico molecular
Country: Reino Unido
Editor: Wiley
Rights: Aberto
Identifier DOI: 10.1002/mgg3.877
Date Issue: Nov-2019
Appears in Collections:FCM - Artigos e Outros Documentos

Files in This Item:
File Description SizeFormat 
000485408200001.pdf599.77 kBAdobe PDFView/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.