Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Hereditary neurological disease · Autosomal recessive disease · Disorder of tyrosine metabolism · Dopa-responsive dystonia · Tyrosine hydroxylase deficiency
TH-deficient dopa-responsive dystonia
Autosomal recessive dopa-responsive dystonia (DYT5b) is a very rare neurometabolic disorder characterized by a spectrum of symptoms ranging from those seen in dopa-responsive dystonia (DRD) to progressive infantile encephalopathy.
This condition has no sub-types.