: Large or deep bruises (hematomas) resulting from minor trauma.
: A rare, non-inherited autoimmune condition where the body’s immune system attacks its own clotting factors. Core Symptoms and Complications
Hemophilia is a rare, typically inherited genetic disorder that impairs the body's ability to form blood clots. This deficiency in clotting factors—proteins essential for stopping blood flow—results in prolonged bleeding after injury or surgery and can lead to spontaneous internal bleeding, particularly into joints and muscles. Primary Classifications hemophilia
: Females usually have two X chromosomes and can be carriers of the gene. While many carriers are asymptomatic, some may experience mild bleeding symptoms.
Hemophilia is generally an disorder, meaning it primarily affects males. : Large or deep bruises (hematomas) resulting from
While there is currently no absolute cure, management has advanced significantly, allowing most patients in developed nations to achieve a near-normal life expectancy.
: The most common form, caused by a lack of Factor VIII (8). It accounts for roughly 80% to 85% of cases. Hemophilia is generally an disorder, meaning it primarily
: Preventive regular infusions to maintain factor levels and prevent joint damage.