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Congenital Afibrinogenemia



Congenital Afibrinogenemia: Introduction

Congenital Afibrinogenemia: A rare disorder involving the inability to make fibrinogen which is essential for the process of blood clotting. More detailed information about the symptoms, causes, and treatments of Congenital Afibrinogenemia is available below.

Symptoms of Congenital Afibrinogenemia

See full list of 10 symptoms of Congenital Afibrinogenemia

Home Diagnostic Testing

Home medical testing related to Congenital Afibrinogenemia:

Congenital Afibrinogenemia: Complications

Review possible medical complications related to Congenital Afibrinogenemia:

Less Common Symptoms of Congenital Afibrinogenemia

Read more about symptoms of Congenital Afibrinogenemia

Wrongly Diagnosed with Congenital Afibrinogenemia?

Congenital Afibrinogenemia: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Congenital Afibrinogenemia

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Read more about Misdiagnosis and Congenital Afibrinogenemia

Congenital Afibrinogenemia: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Hospitals & Clinics: Congenital Afibrinogenemia

Research quality ratings and patient safety measures for medical facilities in specialties related to Congenital Afibrinogenemia:

Hospital & Clinic quality ratings » »

Choosing the Best Hospital: More general information, not necessarily in relation to Congenital Afibrinogenemia, on hospital performance and surgical care quality:

Evidence Based Medicine Research for Congenital Afibrinogenemia

Medical research articles related to Congenital Afibrinogenemia include:

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

Videos for Congenital Afibrinogenemia

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Prognosis for Congenital Afibrinogenemia

Prognosis for Congenital Afibrinogenemia: some survive to adulthood

More about prognosis of Congenital Afibrinogenemia

Reseach about Congenital Afibrinogenemia

Visit our research pages for current research about Congenital Afibrinogenemia treatments.

User Interactive Forums

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Definitions of Congenital Afibrinogenemia:

A rare congenital disorder of blood coagulation in which no fibrinogen is found in the blood plasma - (Source - WordNet 2.1)

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


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