Preliminary observations of glucose metabolism dysregulation in pediatric Huntington’s disease

Preliminary observations of glucose metabolism dysregulation in pediatric Huntington’s disease

BackgroundPediatric Huntington’s disease (PHD), a rare and severe form of juvenile-onset Huntington’s disease (JOHD), is associated with highly expanded CAG repeats in the HTT gene and a rapidly progressive neurodegenerative course. Recent studies have suggested that glucose metabolism may be impair...

Full description

Saved in:
Bibliographic Details
Main Authors: Federica Graziola, Federica Rachele Danti, Martina Penzo, Antonio Spagarino, Eleonora Minacapilli, Marco Moscatelli, Federica Zibordi, Caterina Mariotti, Giovanna Zorzi
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-08-01
Series:Frontiers in Neurology
Subjects:
Huntington’s disease
pediatric Huntington’s disease
juvenile-onset HD
GLUT-1 deficiency syndrome
GLUT1
Online Access:https://www.frontiersin.org/articles/10.3389/fneur.2025.1626275/full
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

https://www.frontiersin.org/articles/10.3389/fneur.2025.1626275/full

Similar Items