Scott Syndrome

Watchlist

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Retrieved

2021-01-23

Source

Orphanet

Trials

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Genes

ANO6, ADAM10, ANXA5, KLK3, FLNB, MYH3, ABCB4, PLAG1, PROS1, NPEPPS, MMD, PSAT1, ANO1, ANO10, ANO5

Drugs

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Scott syndrome is an extremely rare congenital hemorrhagic disorder characterized by hemorrhagic episodes due to impaired platelet coagulant activity.