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What is Von Willebrand disease, type 2M?

What is Von Willebrand disease, type 2M?

  • Von Willebrand disease, type 2M: A rare inherited blood coagulation disorder characterized by a defect in plasma protein called the von Willebrand factor which leads to bleeding problems. Type 2 vWD is further subdivided into 4 subtypes, each with a different underlying genetic defect. Type 2M is very rare. The severity of the bleeding symptoms is variable.

Von Willebrand disease, type 2M: Introduction

Types of Von Willebrand disease, type 2M:

Broader types of Von Willebrand disease, type 2M:

What causes Von Willebrand disease, type 2M?

Causes of Von Willebrand disease, type 2M: see causes of Von Willebrand disease, type 2M

What are the symptoms of Von Willebrand disease, type 2M?

Symptoms of Von Willebrand disease, type 2M: see symptoms of Von Willebrand disease, type 2M

Von Willebrand disease, type 2M: Testing

Diagnostic testing: see tests for Von Willebrand disease, type 2M.

Misdiagnosis: see misdiagnosis and Von Willebrand disease, type 2M.

How is it treated?

Treatments for Von Willebrand disease, type 2M: see treatments for Von Willebrand disease, type 2M

Name and Aliases of Von Willebrand disease, type 2M

Main name of condition: Von Willebrand disease, type 2M

Other names or spellings for Von Willebrand disease, type 2M:

Willebrand disease, type 2M, 2M vWD

 

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