Neurodegenerative Diseases
Genetic, Proteomic and Metabolic Biomarkers for Predicting and Monitoring Huntington’s Disease Progression: A Systematic Review
Gloria Ibis Tirado Romero, Ana María Jiménez Echavarría, Laura Rocío Orrego-Agudelo
touchREVIEWS in Neurology. 2025;21(1):51-62
Huntington’s disease (HD) is a fatal, autosomal-dominant, neurodegenerative disorder caused by a cytosine–adenine–guanine (CAG) trinucleotide repeat expansion in the huntingtin (HTT) gene, located on chromosome 4p16.3. When this repeat exceeds 36 units, it leads to the synthesis of a mutant HTT (mHTT) protein, which aggregates and disrupts numerous cellular processes, including transcriptional regulation, mitochondrial function, axonal transport and […]