Find the best answers to your questions at Westonci.ca, where experts and enthusiasts provide accurate, reliable information. Join our platform to connect with experts ready to provide precise answers to your questions in different areas. Our platform provides a seamless experience for finding reliable answers from a network of experienced professionals.

Classic hemophilia and classic Von Willebrand's disease may have all of the following in common except:
a. Prolonged PT
b. Prolonged PTT
c. Prolonged BleedingTime
d. Factor VIII diminished"


Sagot :

Answer:

Prolonged PT

Prolonged PT is not common to both classic hemophilia and classic von Willebrand's disease.

Explanation:

Classic hemophilia (Hemophilia A) and classic Von Willebrand's disease (vWD) are both disorders that affect blood clotting, but they do so in different ways. Let's analyze the options provided:

a. Prolonged PT (Prothrombin Time): PT is usually normal in both Hemophilia A and vWD because PT measures the extrinsic pathway of coagulation, which is not typically affected by deficiencies in Factor VIII or von Willebrand factor..

b. Prolonged PTT (Partial Thromboplastin Time): PTT is prolonged in both conditions. Hemophilia A involves a deficiency in Factor VIII, which is part of the intrinsic pathway measured by PTT. In vWD, there may also be a prolonged PTT due to the role of von Willebrand factor in stabilizing Factor VIII.

c. Prolonged Bleeding Time: Bleeding time is prolonged in vWD due to the role of von Willebrand factor in platelet adhesion. It may be normal or slightly prolonged in Hemophilia A depending on the severity of the factor deficiency.

d. Factor VIII diminished: In Hemophilia A, Factor VIII is diminished. In vWD, Factor VIII levels can also be reduced because von Willebrand factor protects Factor VIII from rapid degradation.