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What is Bethesda I dysfibrinogenemia?

What is Bethesda I dysfibrinogenemia?

  • Bethesda I dysfibrinogenemia: A rare inherited disorder characterized by abnormal fibrinogen which is a protein essential to the blood clotting process. The Bethesda I type was discovered in Bethesda.

Bethesda I dysfibrinogenemia: Introduction

Types of Bethesda I dysfibrinogenemia:

Broader types of Bethesda I dysfibrinogenemia:

What causes Bethesda I dysfibrinogenemia?

Causes of Bethesda I dysfibrinogenemia: see causes of Bethesda I dysfibrinogenemia

What are the symptoms of Bethesda I dysfibrinogenemia?

Symptoms of Bethesda I dysfibrinogenemia: see symptoms of Bethesda I dysfibrinogenemia

Bethesda I dysfibrinogenemia: Testing

Diagnostic testing: see tests for Bethesda I dysfibrinogenemia.

Misdiagnosis: see misdiagnosis and Bethesda I dysfibrinogenemia.

How is it treated?

Doctors and Medical Specialists for Bethesda I dysfibrinogenemia: Hematologist ; see also doctors and medical specialists for Bethesda I dysfibrinogenemia.
Treatments for Bethesda I dysfibrinogenemia: see treatments for Bethesda I dysfibrinogenemia

Name and Aliases of Bethesda I dysfibrinogenemia

Main name of condition: Bethesda I dysfibrinogenemia

Other names or spellings for Bethesda I dysfibrinogenemia:

dysfibrinogenemia, Bethesda I

 

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