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What is Metz dysfibrinogenemia?

What is Metz dysfibrinogenemia?

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

Metz dysfibrinogenemia: Introduction

Types of Metz dysfibrinogenemia:

Broader types of Metz dysfibrinogenemia:

What causes Metz dysfibrinogenemia?

Causes of Metz dysfibrinogenemia: see causes of Metz dysfibrinogenemia

What are the symptoms of Metz dysfibrinogenemia?

Symptoms of Metz dysfibrinogenemia: see symptoms of Metz dysfibrinogenemia

Metz dysfibrinogenemia: Testing

Diagnostic testing: see tests for Metz dysfibrinogenemia.

Misdiagnosis: see misdiagnosis and Metz dysfibrinogenemia.

How is it treated?

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

Name and Aliases of Metz dysfibrinogenemia

Main name of condition: Metz dysfibrinogenemia

Other names or spellings for Metz dysfibrinogenemia:

dysfibrinogenemia, Metz


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