Tag: Hemophilia c

While severe Factor XI deficiency affects approximately 1 in 1 million people worldwide, its most common presentation is not spontaneous bleeding, but rather delayed or prolonged bleeding following a hemostatic challenge like surgery or trauma. The clinical picture is often unpredictable and does not correlate reliably with the patient's measured factor XI levels.

Approximately 1 in 5,000 male births are affected by hemophilia A, making it the most common form of this rare inherited bleeding disorder. This condition, along with hemophilia B and C, is caused by a deficiency in specific blood clotting factors, but understanding what is the difference between hemophilia A and B and C is crucial for diagnosis and effective management.

Affecting an estimated 1 in 100,000 people globally, factor 11 deficiency is a rare genetic bleeding disorder with a generally favorable prognosis. The condition, also known as hemophilia C, is usually milder than other forms of hemophilia, and most affected individuals can expect to live a normal lifespan with proper care and preventive measures.

Hemophilia is a rare inherited bleeding disorder, with Hemophilia A being the most common type, affecting approximately 1 in 5,000 male live births worldwide. This guide will explain **what are the 4 types of hemophilia** and how they differ.

According to the National Bleeding Disorders Foundation, Hemophilia C, also known as Factor XI deficiency, is a rare bleeding disorder affecting roughly 1 in 100,000 people. To understand the condition, you must know **Which factor is missing in hemophilia C?**

Affecting an estimated 1 in 5 million people, Factor XIII deficiency, also known as fibrin-stabilizing factor deficiency, is truly the rarest inherited form of hemophilia, setting it apart from the more common types A and B.