Bernard-Soulier Syndrome
Watchlist
Retrieved
2021-01-23
Source
Trials
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Genes
GP1BA,
GP1BB,
GP9,
SEPTIN5,
VWF,
CHRNE,
PRB2,
GP5,
SEPT5-GP1BB,
ITGA2B,
FGFR2,
ABCB6,
PRNP,
C4BPA,
MYH9,
PRDX2,
CARD14,
NLRP3,
AHSA1,
RNF19A,
THPO,
POLDIP2,
ADIPOQ,
AIMP2,
XYLT1,
TRAP,
QRSL1,
TPO,
GRAP2,
C3
GP1BA,
GP1BB,
GP9,
SEPTIN5,
VWF,
CHRNE,
PRB2,
GP5,
SEPT5-GP1BB,
ITGA2B,
FGFR2,
ABCB6,
PRNP,
C4BPA,
MYH9,
PRDX2,
CARD14,
NLRP3,
AHSA1,
RNF19A,
THPO,
POLDIP2,
ADIPOQ,
AIMP2,
XYLT1,
TRAP,
QRSL1,
TPO,
GRAP2,
C3,
RYR1,
MAPK1,
LGALS8,
ITGB3,
ITGB1,
ITGA2,
IL4R,
IL1B,
FN1,
FBLN1,
F11,
F2,
MAPK14,
CRK,
CASP1,
PF4
Drugs
—
Registered!
Bernard Soulier syndrome (BSS) is an inherited platelet disorder characterized by mild to severe bleeding tendency , macrothrombocytopenia and absent ristocetin-induced platelet agglutination.