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What is Bethesda II dysfibrinogenemia?

What is Bethesda II dysfibrinogenemia?

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

Bethesda II dysfibrinogenemia: Introduction

Types of Bethesda II dysfibrinogenemia:

Broader types of Bethesda II dysfibrinogenemia:

What causes Bethesda II dysfibrinogenemia?

Causes of Bethesda II dysfibrinogenemia: see causes of Bethesda II dysfibrinogenemia

What are the symptoms of Bethesda II dysfibrinogenemia?

Symptoms of Bethesda II dysfibrinogenemia: see symptoms of Bethesda II dysfibrinogenemia

Bethesda II dysfibrinogenemia: Testing

Diagnostic testing: see tests for Bethesda II dysfibrinogenemia.

Misdiagnosis: see misdiagnosis and Bethesda II dysfibrinogenemia.

How is it treated?

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

Name and Aliases of Bethesda II dysfibrinogenemia

Main name of condition: Bethesda II dysfibrinogenemia

Other names or spellings for Bethesda II dysfibrinogenemia:

dysfibrinogenemia, Bethesda II


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