Cargando…
Over 20-Year Follow-up of Patients with Hepatic Glycogen Storage Diseases: Single-Center Experience
Background: The published data on the long-term outcomes of glycogen storage disease (GSD) patients is sparse in the literature. The aim of this study was to analyze the long-term (over 20 years) follow-up of patients with hepatic types of GSD-I, III, VI, and IX—from childhood to adulthood, managed...
Autores principales: | Szymańska, Edyta, Lipiński, Patryk, Rokicki, Dariusz, Książyk, Janusz, Tylki-Szymańska, Anna |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7277974/ https://www.ncbi.nlm.nih.gov/pubmed/32414085 http://dx.doi.org/10.3390/diagnostics10050297 |
Ejemplares similares
-
Hepatic glycogen storage diseases: pathogenesis, clinical symptoms and therapeutic management
por: Szymańska, Edyta, et al.
Publicado: (2019) -
Clinical, biochemical and molecular phenotype of congenital disorders of glycosylation: long-term follow-up
por: Bogdańska, Anna, et al.
Publicado: (2021) -
ATP6AP1‐CDG: Follow‐up and female phenotype
por: Lipiński, Patryk, et al.
Publicado: (2020) -
Outcomes of oral biotin treatment in patients with biotinidase deficiency — Twenty years follow-up
por: Szymańska, Edyta, et al.
Publicado: (2015) -
Pediatric patient with hyperketotic hypoglycemia diagnosed with glycogen synthase deficiency due to the novel homozygous mutation in GYS2
por: Szymańska, Edyta, et al.
Publicado: (2015)