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Dysfibrinogenemia, familial

Dysfibrinogenemia, familial: Introduction

Dysfibrinogenemia, familial: A rare familial disorder characterized by abnormal fibrinogen. There are various types of this order and they can vary in severity from asymptomatic to causing abnormal bleeding and blood clotting. Examples of subtypes includes Amsterdam, Detroit and Wiesbaden dysfibrinogenemia. More detailed information about the symptoms, causes, and treatments of Dysfibrinogenemia, familial is available below.

Symptoms of Dysfibrinogenemia, familial

Home Diagnostic Testing

Home medical testing related to Dysfibrinogenemia, familial:

Wrongly Diagnosed with Dysfibrinogenemia, familial?

Causes of Dysfibrinogenemia, familial

Read more about causes of Dysfibrinogenemia, familial.

Misdiagnosis and Dysfibrinogenemia, familial

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 the condition tend to have more »

Dysfibrinogenemia, familial: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Dysfibrinogenemia, familial: Animations

Statistics for Dysfibrinogenemia, familial

Dysfibrinogenemia, familial: Broader Related Topics

User Interactive Forums

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Definitions of Dysfibrinogenemia, familial:

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Dysfibrinogenemia, familial as a "rare disease".
Source - Orphanet

Related Dysfibrinogenemia, familial Info

More information about Dysfibrinogenemia, familial

  1. Dysfibrinogenemia, familial: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing

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