Kufor-Rakeb Syndrome

Watchlist

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Retrieved

2021-01-23

Source

Orphanet

Trials

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Genes

ATP13A2, SNCA, KARS1, PLA2G1B, SLC6A3, YWHAZ, EGLN1, FA2H, PANK2, LRRK2, PLB1

Drugs

Deferiprone ( FERRIPROX, DEFERIPRONE LIPOMED )

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Kufor-Rakeb syndrome (KRS) is a rare genetic neurodegenerative disorder characterized by juvenile Parkinsonism, pyramidal degeneration (dystonia), supranuclear palsy, and cognitive impairment.