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T. Loboda

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Case report Open access Aug 2026

Early Manifestations, Diagnostic Pathways, and Epilepsy in Juvenile-Onset Huntington Disease: A Three-Patient Case Series and Systematic Review

Highlights What are the main findings? Juvenile-onset Huntington disease frequently presented with heterogeneous, non-choreic developmental, psychiatric, gait, speech, and movement abnormalities, with a median diagnostic delay of 4 years. Among published patients with ascertainable seizure status, epilepsy was reported...

Mirjana Perkovič Benedik, T. Loboda, Katarina Benedik Kafol et al. · 0 citations

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