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Hemophilia A

Hemophilia A: Introduction

Hemophilia A: Hemophilia A is a hereditary blood disorder, primarily affecting males, characterized by a deficiency of the blood clotting protein known as Factor VIII that results in abnormal ... more about Hemophilia A.

Hemophilia A: A rare coagulation disorder caused by a deficiency of factor VIII which results in bleeding problems. More detailed information about the symptoms, causes, and treatments of Hemophilia A is available below.

Symptoms of Hemophilia A

Home Diagnostic Testing

Home medical testing related to Hemophilia A:

Wrongly Diagnosed with Hemophilia A?

Hemophilia A: Related Patient Stories

Hemophilia A: Complications

Review possible medical complications related to Hemophilia A:

Causes of Hemophilia A

Read more about causes of Hemophilia A.

Disease Topics Related To Hemophilia A

Research the causes of these diseases that are similar to, or related to, Hemophilia A:

Misdiagnosis and Hemophilia A

Unnecessary hysterectomies due to undiagnosed bleeding disorder in women: The bleeding disorder called Von Willebrand's disease is quite common in women, but often fails to be correctly diagnosed. Women with more »

Hemophilia A: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Evidence Based Medicine Research for Hemophilia A

Medical research articles related to Hemophilia A include:

Click here to find more evidence-based articles on the TRIP Database

Hemophilia A: Animations

Research about Hemophilia A

Visit our research pages for current research about Hemophilia A treatments.

Clinical Trials for Hemophilia A

The US based website lists information on both federally and privately supported clinical trials using human volunteers.

Some of the clinical trials listed on for Hemophilia A include:

Statistics for Hemophilia A

Hemophilia A: Broader Related Topics

User Interactive Forums

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Article Excerpts about Hemophilia A

Hemophilia A is a hereditary blood disorder, primarily affecting males, characterized by a deficiency of the blood clotting protein known as Factor VIII that results in abnormal bleeding. Babylonian Jews first described hemophilia more than 1700 years ago; the disease first drew widespread public attention when Queen Victoria transmitted it to several European royal families. (Source: Genes and Disease by the National Center for Biotechnology)

Definitions of Hemophilia A:

An inherited deficiency of coagulation Factor VIII characterized by the tendency to spontaneous or exaggerated post-traumatic hemorrhage. Inherited as an x-linked recessive disease, hemophilia A is the most common hemophilia, occurring in approximately 1 in 10,000 male births. --2004 - (Source - Diseases Database)

Hemophilia A is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Hemophilia A, or a subtype of Hemophilia A, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)


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