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Familial erythrocytosis, 2

Familial erythrocytosis, 2: Introduction

Familial erythrocytosis, 2: A rare genetic blood disorder resulting in an increased red blood cell count. The genetic mutation occurs on the VHL gene on chromosome 3p26-p25. More detailed information about the symptoms, causes, and treatments of Familial erythrocytosis, 2 is available below.

Symptoms of Familial erythrocytosis, 2

  • Increased red blood cell count
  • Increased hemoglobin concentration
  • Low serum erythropoietin level
  • Headache
  • Increased risk of peripheral thrombosis
  • more symptoms...»

Home Diagnostic Testing

Home medical testing related to Familial erythrocytosis, 2:

Wrongly Diagnosed with Familial erythrocytosis, 2?

Causes of Familial erythrocytosis, 2

Read more about causes of Familial erythrocytosis, 2.

Misdiagnosis and Familial erythrocytosis, 2

Unnecessary hysterectomies due to undiagnosed bleeding disorder in women: The bleeding disorder called Von Willebrand's disease is quite common in women, but often fails to be correctly...read more »

Familial erythrocytosis, 2: Research Doctors & Specialists

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Familial erythrocytosis, 2: Animations

Familial erythrocytosis, 2: Broader Related Topics

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Related Familial erythrocytosis, 2 Info

More information about Familial erythrocytosis, 2

  1. Familial erythrocytosis, 2: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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