DYT12 (Dystonia-12) is a rare genetic movement disorder, primarily known as (RDP). It is characterized by the sudden appearance of movement symptoms, often triggered by severe physical or emotional stress. 🧬 Clinical Review of DYT12
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: Mutations in the ATP1A3 gene , which provides instructions for a subunit of a protein pump critical for normal neuron signaling.
: Significant difficulty with speaking ( dysarthria ) and swallowing ( dysphagia ).
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