Symptomatic Form Of Hemophilia A In Female Carriers
Watchlist
Retrieved
2021-01-23
Source
Trials
—
Genes
F8,
F9,
TFPI,
F10,
AK3,
F2,
VWF,
COX8A,
ST14,
F5,
F3,
PROC,
IL10,
CCR5,
AAVS1,
HLA-DRB1,
TNF,
MS4A1,
CCND1,
GP1BA,
G6PD,
LMAN1,
RBM45,
KRT20,
ABO,
CPB2,
VIPR1,
PROCR,
ISG20,
IFNA2
F8,
F9,
TFPI,
F10,
AK3,
F2,
VWF,
COX8A,
ST14,
F5,
F3,
PROC,
IL10,
CCR5,
AAVS1,
HLA-DRB1,
TNF,
MS4A1,
CCND1,
GP1BA,
G6PD,
LMAN1,
RBM45,
KRT20,
ABO,
CPB2,
VIPR1,
PROCR,
ISG20,
IFNA2,
IL2,
TGFB1,
IL2RA,
SELP,
IL4,
IFNL3,
MAPK9,
PF4,
HAL,
PROS1,
FOXP3,
STATH,
PRNP,
ADAMTS5,
WDHD1,
MTHFR,
F7,
AMBP,
ABR,
DMD,
ALB,
GH1,
ARTN,
DKK1,
APOH,
BPI,
BRCA1,
ABCB6,
CD163,
FCGR2C,
TNFRSF11A,
HAP1,
TRBV16,
IKBKG,
SLC14A2,
LAP,
BTK,
C4BPA,
VEGFA,
TPT1,
C6,
THBD,
NT5C2,
HFE,
TRBV7-9,
CALR,
MIR1246,
C20orf181,
C4orf3,
CA13,
ASPG,
AGRP,
IL33,
MCFD2,
CARD14,
FUNDC2,
UPF3B,
HPSE2,
IMPACT,
SCLY,
SERPINA10,
SOST,
APC,
ICOS,
TRBC1,
CA6,
TRBV20OR9-2,
PRDX2,
FUT1,
LTF,
LRP1,
F11,
KRT7,
KIT,
FCGR2A,
FCGR2B,
CXCL8,
IL6,
UTS2R,
HLA-A,
IL1B,
IFNG,
GPT,
ICAM1,
HNF4A,
HMOX1,
GUSB,
HLA-DRA,
HLA-B,
MBL2,
MRC1,
NFYA,
NHS,
TRB,
TAL1,
CD28,
CD68,
SPRR2A,
SLC4A1,
SELPLG,
CLTC,
CCL3L1,
REST,
PSMA7,
CSF1R,
CSF2,
CTLA4,
SERPINE2,
DPP4,
SERPINA5,
SERPINE1,
TNFRSF11B,
MIR4521
Drugs
—
Registered!

Symptomatic hemophilia A in female carriers is a form of hemophilia A (see this term) that manifests in some women with mutations in the F8 gene (Xq28), encoding coagulation factor VIII.
Epidemiology
Prevalence is unknown but this form of hemophilia is very rare.
Clinical description
Symptoms include abnormal bleeding as a result of minor injuries, or following surgery or tooth extraction. Spontaneous hemorrhages may occur occasionally.
Genetic counseling
Transmission is X-linked recessive.