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What is Fibrinogen deficiency, congenital?

What is Fibrinogen deficiency, congenital?

  • Fibrinogen deficiency, congenital: A rare congenital disorder characterized by the inability to make fibrinogen which is essential for the process of blood clotting.

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Fibrinogen deficiency, congenital as a "rare disease".
Source - Orphanet

Fibrinogen deficiency, congenital: Introduction

Types of Fibrinogen deficiency, congenital:

Broader types of Fibrinogen deficiency, congenital:

How serious is Fibrinogen deficiency, congenital?

Prognosis of Fibrinogen deficiency, congenital: some survive to adulthood
Complications of Fibrinogen deficiency, congenital: see complications of Fibrinogen deficiency, congenital

What causes Fibrinogen deficiency, congenital?

Causes of Fibrinogen deficiency, congenital: see causes of Fibrinogen deficiency, congenital

What are the symptoms of Fibrinogen deficiency, congenital?

Symptoms of Fibrinogen deficiency, congenital: see symptoms of Fibrinogen deficiency, congenital

Complications of Fibrinogen deficiency, congenital: see complications of Fibrinogen deficiency, congenital

Onset of Fibrinogen deficiency, congenital: birth

Fibrinogen deficiency, congenital: Testing

Diagnostic testing: see tests for Fibrinogen deficiency, congenital.

Misdiagnosis: see misdiagnosis and Fibrinogen deficiency, congenital.

How is it treated?

Doctors and Medical Specialists for Fibrinogen deficiency, congenital: Hematologist ; see also doctors and medical specialists for Fibrinogen deficiency, congenital.
Treatments for Fibrinogen deficiency, congenital: see treatments for Fibrinogen deficiency, congenital

Name of Fibrinogen deficiency, congenital

Main name of condition: Fibrinogen deficiency, congenital

 

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