Bleeding occurs because factor VIII? - faster

[ArchivalUser]

Patients with hemophilia A (ie., factor VIII deficiency)
have a bleeding disorder. Bleeding occurs because
factor VIII
(A) Acts as a reaction accelerator (cofactor) during the
activation of a coagulation factor
(B) Provides the phospholipid necessary for assembly of
coagulation factors, cofactors, and calcium
© Promotes platelet aggregation
(D) Neutralizes antithrombin III
(E) Causes platelets to release thromboxane A2

[ArchivalUser]

a ?

[ArchivalUser]

A...FVIIIa is the co-factor of FIXa, and together they form the "tenase" complex, which activates FX; and so the cycle continues.

[ArchivalUser]

My email address : heyharshal@ymail.com

[ArchivalUser]

aaa

[ArchivalUser]

AA IS RIGHT

[ArchivalUser]

explanation please

[ArchivalUser]

(A) Factor VIII, tissue factor, and factor V act as
cofactors or reaction accelerators in the clotting cascade.
Factor VIII acts as a reaction accelerator for the conversion
of factor X and Xa. The platelet surface provides phospholipid
for assembly of coagulation factors. Platelet aggregation
is promoted by thromboxane A, and ADP. Thromboxane
A2 is released when platelets are activated during the
process of platelet adhesion.

[ArchivalUser]

Oye Punjabidoc,Upar explanation likha hai yaarrr... dekha nahi kya?