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What is Factor XI deficiency, congenital?

What is Factor XI deficiency, congenital?

  • Factor XI deficiency, congenital: A rare inherited bleeding disorder characterized by a deficiency of a blood protein called Factor XI which is needed for the blood clotting process. The condition is generally quite mild but the severity of the condition is variable.

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

Factor XI deficiency, congenital: Introduction

Types of Factor XI deficiency, congenital:

Broader types of Factor XI deficiency, congenital:

Who gets Factor XI deficiency, congenital?

Racial predominance for Factor XI deficiency, congenital: European Jews and Japanese

How serious is Factor XI deficiency, congenital?

Prognosis of Factor XI deficiency, congenital: variable according to severity
Complications of Factor XI deficiency, congenital: see complications of Factor XI deficiency, congenital

What causes Factor XI deficiency, congenital?

Causes of Factor XI deficiency, congenital: see causes of Factor XI deficiency, congenital

What are the symptoms of Factor XI deficiency, congenital?

Symptoms of Factor XI deficiency, congenital: see symptoms of Factor XI deficiency, congenital

Complications of Factor XI deficiency, congenital: see complications of Factor XI deficiency, congenital

Can anyone else get Factor XI deficiency, congenital?

Inheritance: see inheritance of Factor XI deficiency, congenital

Factor XI deficiency, congenital: Testing

Diagnostic testing: see tests for Factor XI deficiency, congenital.

Misdiagnosis: see misdiagnosis and Factor XI deficiency, congenital.

How is it treated?

Doctors and Medical Specialists for Factor XI deficiency, congenital: Medical Geneticist ; see also doctors and medical specialists for Factor XI deficiency, congenital.
Treatments for Factor XI deficiency, congenital: see treatments for Factor XI deficiency, congenital

Name and Aliases of Factor XI deficiency, congenital

Main name of condition: Factor XI deficiency, congenital

Other names or spellings for Factor XI deficiency, congenital:

Rosenthal (R.L.) syndrome, hemophilia C, PTA deficiency, Plasma thromboplastin antecedent deficiency, Factor XI deficiency, F11 deficiency, Rosenthal syndrome

Factor XI deficiency, congenital: Related Conditions

Research the causes of these diseases that are similar to, or related to, Factor XI deficiency, congenital:

 

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