Original article
Glycogen storage disease type I: clinical and laboratory profile
Doença de depósito de glicogênio tipo I: perfil clínico e laboratorial
Berenice L. Santosa, Carolina F.M. de Souzab, Lavinia Schuler-Faccinia,b,c, Lilia Refoscob, Matias Epifaniod,e, Tatiele Nalinf, Sandra M.G. Vieirag,h, Ida V.D. Schwartzb,c,
Corresponding author
a Post-Graduate Program in Child and Adolescent Health, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, RS, Brazil
b Medical Genetics Service, Hospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brazil
c Department of Genetics, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, RS, Brazil
d Pontifícia Universidade Católica do Rio Grande do Sul (PUC-RS), Porto Alegre, RS, Brazil
e Hospital São Lucas, Porto Alegre, RS, Brazil
f Post-Graduate Program in Genetics and Molecular Biology, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, RS, Brazil
g Medical Pediatric Service, Hospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brazil
h Post-Graduate Program in Gastroenterology Science and Hepatology, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, RS, Brazil
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