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Up to: Hereditary peripheral neuropathy · Thiamine-responsive dysfunction syndrome
Progressive demyelinating neuropathy with bilateral striatal necrosis
Progressive polyneuropathy with bilateral striatal necrosis is a rare, genetic disorder of thiamine metabolism and transport characterized by the childhood-onset of recurrent episodes of flaccid paralysis and encephalopathy, associated with bilateral striatal necrosis and chronic progressive axonal polyneuropathy with proximal and distal muscle weakness, areflexia, contractures and foot deformities.
This condition has no sub-types.