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What is Dysfibrinogenemia, familial?

What is Dysfibrinogenemia, familial?

  • 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.

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

Dysfibrinogenemia, familial: Introduction

Types of Dysfibrinogenemia, familial:

Broader types of Dysfibrinogenemia, familial:

What causes Dysfibrinogenemia, familial?

Causes of Dysfibrinogenemia, familial: see causes of Dysfibrinogenemia, familial

What are the symptoms of Dysfibrinogenemia, familial?

Symptoms of Dysfibrinogenemia, familial: see symptoms of Dysfibrinogenemia, familial

Dysfibrinogenemia, familial: Testing

Diagnostic testing: see tests for Dysfibrinogenemia, familial.

Misdiagnosis: see misdiagnosis and Dysfibrinogenemia, familial.

How is it treated?

Doctors and Medical Specialists for Dysfibrinogenemia, familial: Medical Geneticist, Hematologist ; see also doctors and medical specialists for Dysfibrinogenemia, familial.
Treatments for Dysfibrinogenemia, familial: see treatments for Dysfibrinogenemia, familial

Name of Dysfibrinogenemia, familial

Main name of condition: Dysfibrinogenemia, familial

 

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