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==Overview==
==Overview==
[[Hemophilia A]] is caused by an inherited [[X-linked]] [[recessive trait]], with the defective [[gene]] located on the [[X chromosome]].
==Causes==
==Causes==
[[Hemophilia B]] is caused by an inherited [[X-linked]] [[recessive trait]], with the defective [[gene]] located on the [[X chromosome]].
Females have two copies of the [[X chromosome]], so if the [[factor VIII]] [[gene]] on one [[chromosome]] is defective, the [[gene]] on the other [[chromosome]] can do the job of making enough [[factor VIII]].
 
Females have two copies of the [[X chromosome]], so if the [[factor IX]] [[gene]] on one [[chromosome]] is defective, the [[gene]] on the other [[chromosome]] can do the job of making enough [[factor IX]].


Males, however, have only one [[X chromosome]], so if the [[factor IX]] [[gene]] on that [[chromosome]] is defective, they will have [[Hemophilia B]]. Therefore, most people with [[hemophilia B]] are male.
Males, however, have only one [[X chromosome]], so if the [[factor VIII]] [[gene]] on that [[chromosome]] is defective, they will have [[Hemophilia A]]. Therefore, most people with [[hemophilia A]] are male.


If a woman has a defective [[factor IX]] [[gene]], she is considered a carrier. This means the defective [[gene]] can be passed down to her children.
If a woman has a defective [[factor VIII]] [[gene]], she is considered a carrier. This means the defective [[gene]] can be passed down to her children.


Boys born to a woman who carries the defective [[gene]] have a 50% chance of having [[hemophilia B]], while their daughters have a 50% chance of  being a carrier.
Boys born to a woman who carries the defective [[gene]] have a 50% chance of having [[hemophilia A]], while their daughters have a 50% chance of  being a carrier.


All female children of men with [[hemophilia]] carry the defective [[gene]].
All female children of men with [[hemophilia A]] carry the defective [[gene]].


==References==
==References==

Revision as of 07:10, 27 March 2017

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Fahd Yunus, M.D. [2]

Overview

Hemophilia A is caused by an inherited X-linked recessive trait, with the defective gene located on the X chromosome.

Causes

Females have two copies of the X chromosome, so if the factor VIII gene on one chromosome is defective, the gene on the other chromosome can do the job of making enough factor VIII.

Males, however, have only one X chromosome, so if the factor VIII gene on that chromosome is defective, they will have Hemophilia A. Therefore, most people with hemophilia A are male.

If a woman has a defective factor VIII gene, she is considered a carrier. This means the defective gene can be passed down to her children.

Boys born to a woman who carries the defective gene have a 50% chance of having hemophilia A, while their daughters have a 50% chance of being a carrier.

All female children of men with hemophilia A carry the defective gene.

References

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