Sphingolipidoses and Retinal Involvement: A Comprehensive Review

Sphingolipidoses are a class of inherited lysosomal storage diseases, characterized by enzymatic deficiencies that impair sphingolipid degradation. This enzymatic malfunction results in the pathological accumulation of sphingolipids within lysosomes, leading to tissue damage across multiple organ sy...

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Bibliographic Details
Main Authors: Chiara Carrozzi, Daniele Fumi, Davide Fasciolo, Federico Di Tizio, Serena Fragiotta, Mariachiara Di Pippo, Solmaz Abdolrahimzadeh
Format: Article
Language:English
Published: MDPI AG 2025-03-01
Series:Applied Sciences
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Online Access:https://www.mdpi.com/2076-3417/15/5/2863
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