Clinical and imaging predictors of late‐onset GM2 gangliosidosis: A scoping review

Clinical and imaging predictors of late‐onset GM2 gangliosidosis: A scoping review

Abstract Objective Late‐onset GM2 gangliosidosis (LOGG) subtypes late‐onset Tay‐Sachs (LOTS) and Sandhoff disease (LOSD) are ultra‐rare neurodegenerative lysosomal storage disorders presenting with weakness, ataxia, and neuropsychiatric symptoms. Previous studies considered LOTS and LOSD clinically...

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Bibliographic Details
Main Authors: Neha P. Godbole, Elizabeth Haxton, Olivia E. Rowe, Joseph J. Locascio, Jeremy D. Schmahmann, Florian S. Eichler, Eva‐Maria Ratai, Christopher D. Stephen
Format: Article
Language:English
Published: Wiley 2024-01-01
Series:Annals of Clinical and Translational Neurology
Online Access:https://doi.org/10.1002/acn3.51947

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https://doi.org/10.1002/acn3.51947

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