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.· Brain Science· 0 citations
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