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Up to: Hereditary skin disorder · Hereditary peripheral neuropathy · Epidermal disease · Neuroacanthocytosis

VPS13A-related neurodegenerative disease

A form of neuroacanthocytosis and is characterized clinically by a Huntington disease-like phenotype with progressive neurological symptoms including movement disorders, psychiatric manifestations and cognitive disturbances, and caused by a variation in the VPS13A gene.

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