Hemophilia is a hereditary bleeding disorder caused by missing clotting factors, primarily impacting males. Symptoms include easy bruising and serious bleeding issues. Diagnosis involves blood tests, and treatment centers on replacing clotting factors to prevent bleeding episodes. Early detection and management improve patient outcomes and life quality.

An In-depth Look at Hemophilia: Causes, Symptoms, Detection, and Care Options

Hemophilia is a uncommon inherited disorder that impairs the blood's ability to clot effectively. It stems from a lack of essential clotting proteins, increasing the risk of bleeding both inside and outside the body. Usually inherited, hemophilia can also develop due to new mutations. It predominantly affects males through X-linked inheritance. The main types are Hemophilia A and B, caused by deficiencies in clotting factors VIII and IX. Symptoms include easy bruising and severe bleeding, with diagnosis based on blood tests. Treatment involves replacing deficient factors and managing bleeding, enhancing patients' quality of life.