Hemophilia A causes: Difference between revisions

Jump to navigation Jump to search
(Created page with "__NOTOC__ {{Hemophilia A}} Please help WikiDoc by adding content here. It's easy! Click here to learn about editing. ==References== {{Reflis...")
 
No edit summary
Line 1: Line 1:
__NOTOC__
__NOTOC__
{{Hemophilia A}}
{{Hemophilia A}}
{{CMG}}


Please help WikiDoc by adding content hereIt's easy!  Click  [[Help:How_to_Edit_a_Page|here]] to learn about editing.
==Overview==
==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 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.
 
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.
 
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.
 
All female children of men with [[hemophilia]] carry the defective [[gene]].


==References==
==References==

Revision as of 15:25, 21 September 2012

Hemophilia A Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Hemophilia A from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X Ray

CT

MRI

Echocardiography or Ultrasound

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Hemophilia A causes On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Hemophilia A causes

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Hemophilia A causes

CDC on Hemophilia A causes

Hemophilia A causes in the news

Blogs on Hemophilia A causes

Directions to Hospitals Treating Hemophilia A

Risk calculators and risk factors for Hemophilia A causes

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

Overview

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 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.

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.

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.

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

References

Template:WH Template:WS