Mitochondrial Dysfunction and Its Potential Molecular Interplay in Hypermobile Ehlers–Danlos Syndrome: A Scoping Review Bridging Cellular Energetics and Genetic Pathways

Mitochondrial Dysfunction and Its Potential Molecular Interplay in Hypermobile Ehlers–Danlos Syndrome: A Scoping Review Bridging Cellular Energetics and Genetic Pathways

Hypermobile Ehlers–Danlos Syndrome (hEDS) is a hereditary connective tissue disorder characterized by joint hypermobility, skin hyperextensibility, and systemic manifestations such as chronic fatigue, gastrointestinal dysfunction, and neurological symptoms. Unlike other EDS subtypes with known genet...

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Bibliographic Details
Main Authors: Purusha Shirvani, Arash Shirvani, Michael F. Holick
Format: Article
Language:English
Published: MDPI AG 2025-02-01
Series:Current Issues in Molecular Biology
Subjects:
hypermobile Ehlers–Danlos Syndrome
mitochondrial dysfunction
oxidative phosphorylation
reactive oxygen species
genetic mutations
molecular pathways
Online Access:https://www.mdpi.com/1467-3045/47/2/134
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