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Up to: Hereditary neurological disease · Basal ganglia disorder · Thiamine-responsive dysfunction syndrome
Biotin-responsive basal ganglia disease
Any thiamine-responsive dysfunction syndrome in which the cause of the disease is a variation in the SLC19A3 gene, characterized by subacute encephalopathy with confusion, seizures, and movement disorder, often following a history of febrile illness.
This condition has no sub-types.