ہیوموفیلیا ایک موروثی بیماری ہے جس میں خون جمنے کے عمل میں خرابی پیدا ہو جاتی ہے۔ اس کے نتیجے میں معمولی چوٹ یا زخم بھی زیادہ دیر تک خون بہنے کا سبب بن سکتے ہیں۔ یہ بیماری عموماً پیدائشی ہوتی ہے اور زیادہ تر مردوں کو متاثر کرتی ہے۔ اگر بروقت علاج نہ کیا جائے تو ہیوموفیلیا خطرناک پیچیدگیوں کا باعث بن سکتا ہے۔
Gastroenterologist, Hematologist
MBBS, MCPS (Family Medicine), MD (Internal Medicine)
Hematologist
MBBS, M.Phil. (Hematology), Diploma in Clinical Pathology
Hematologist, Haemoncologist
MBBS, FRCP (London), Certificate of Competence in Lymphoma , MD (UK, FECO (Europe), Haemostasis Acad (UK) , Haemophilia Acad (Edin, UK) , Senior Fellow Bone Marrow Transplantation
Hematologist
MBBS, MCPS Pathology, FCPS Haematology, M.Phil. Haematology/ Pathology
Pediatric Oncologist and Hematologist
MBBS, FCPS (Pediatrics)
Hemophilia is a rare genetic condition where the blood doesn’t clot properly due to a lack of specific clotting factors. Normally, these factors help stop bleeding when you get injured. However, in people with hemophilia, even a small cut or injury can cause prolonged bleeding. In severe cases, bleeding can happen inside the body (in joints, muscles, or vital organs ) which can be life-threatening.
Symptoms of hemophilia vary depending on how severe the condition is. Common signs include:
Hemophilia is caused by a genetic mutation that affects the body’s ability to produce clotting factors. It is usually passed from parents to children through the X chromosome.
Some factors can increase the likelihood of developing hemophilia, such as:
Hemophilia itself cannot be prevented since it is genetic, but complications can be minimized with:
Following are the common types of hemophilia, based on which clotting factor is missing:
This type of hemophilia is caused by a deficiency of clotting factor VIII. This is the most common type.
This hemophilia is caused by a deficiency of clotting factor IX. It is less common but has similar symptoms.
This type involves a lack of clotting factor XI and usually causes mild bleeding.
Doctors diagnose hemophilia through a detailed medical history, physical examination, and lab tests that measure clotting factor levels. Common diagnostic tests include:
Early diagnosis helps in managing bleeding risks and preventing joint or organ damage.
Hemophilia cannot be completely cured, but it can be effectively managed with proper treatment. The main goal of treatment is to replace the missing clotting factor and prevent bleeding episodes before they become serious.
This is the most common treatment. It involves injecting a clotting factor concentrate into the bloodstream to help the blood clot properly. These factors can be made from donated blood or created artificially in laboratories.
This medicine helps the body release extra amounts of the clotting factor (factor VIII) that is already stored in the body. It’s usually given through an injection or nasal spray for mild cases.
These medicines prevent blood clots from breaking down too early. They are usually used before dental treatments or surgeries to control bleeding.
Repeated bleeding into joints can cause pain and stiffness. Physical therapy helps strengthen muscles, improve joint movement, and prevent long-term damage.
This is a newer treatment being researched. It aims to correct the defective gene responsible for hemophilia so the body can start producing clotting factors naturally in the future.
If not properly treated, hemophilia may lead to serious complications, including:
If you or your child has unexplained bleeding or frequent bruising, consult a hematologist immediately. Early diagnosis and treatment can prevent long-term complications. Book an appointment with the best hematologists in Pakistan through Marham today.
The information provided above is for educational purposes only and should not be taken as medical advice. Always consult a qualified healthcare provider for diagnosis and treatment of any medical condition.