Echocardiographic Assessment of Patients with Glycogen Storage Disease in a Single Center

Glycogen storage disease (GSD) is a hereditary metabolic disorder caused by enzyme deficiency resulting in glycogen accumulation in the liver, muscle, heart, or kidney. GSD types II, III, IV, and IX are associated with cardiac involvement. However, cardiac manifestation in other GSD types is unclear...

Descripción completa

Detalles Bibliográficos
Autores principales: Seol, Jaehee, Jung, Seyong, Koh, Hong, Jung, Jowon, Kang, Yunkoo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9916218/
https://www.ncbi.nlm.nih.gov/pubmed/36767559
http://dx.doi.org/10.3390/ijerph20032191

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9916218/
https://www.ncbi.nlm.nih.gov/pubmed/36767559
http://dx.doi.org/10.3390/ijerph20032191

Ejemplares similares