7 Facts You Need to Know About Childhood Hemophilia
What is Childhood Hemophilia?
Childhood Hemophilia is a rare genetic disorder that prevents blood from clotting properly in kids.
Hemophilia is Genetic
Hemophilia is passed down from parents, primarily affecting boys due to X-linked inheritance.
Two Types of Hemophilia
Children may have Hemophilia A (factor VIII deficiency) or Hemophilia B (factor IX deficiency).
Common Symptoms in Children
Symptoms include frequent nosebleeds, bruising easily, and prolonged bleeding from minor injuries.
Diagnosis of Hemophilia
Blood tests measure clotting factors to confirm hemophilia in children. Early diagnosis is crucial.
Treating Hemophilia in Kids
Treatment includes regular infusions of clotting factors to prevent severe bleeding episodes.
Complications of Hemophilia
Untreated hemophilia can lead to joint damage, severe internal bleeding, and mobility issues.
Children Can Live Normal Lives
With proper treatment and care, kids with hemophilia can enjoy active, healthy childhoods.
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