خون کے جمنے کا موروثی مرض، جسے وون ولی برانڈ ڈزیز کہا جاتا ہے، ایک ایسی بیماری ہے جس میں خون کے جمنے میں مدد دینے والا ایک خاص پروٹین کم یا کمزور ہوتا ہے۔ اس کی وجہ سے چھوٹی چوٹ پر بھی خون زیادہ بہنے لگتا ہے اور خواتین میں ماہواری بہت زیادہ ہو سکتی ہے۔ یہ بیماری زیادہ تر والدین سے بچوں میں منتقل ہوتی ہے۔ بروقت تشخیص اور علاج سے مریض ایک معمول کی زندگی گزار سکتا ہے۔
Gastroenterologist, Hematologist
MBBS, MCPS (Family Medicine), MD (Internal Medicine)
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
Von Willebrand disease meaning in Urdu is "خون کے جمنے کا موروثی مرض". It is a lifelong bleeding disorder in which the blood does not clot properly. People with this condition have low levels of a clotting protein called von Willebrand factor, or the protein does not work as it should. This makes it harder for the body to stop bleeding after an injury or surgery.
Von Willebrand disease is the most common inherited bleeding disorder. It affects both men and women in equal numbers, however women usually notice symptoms more because of heavy menstrual bleeding. Most cases are mild and many people do not know they have it until they have a surgery or major injury. There is no cure, however treatment and self-care can prevent and control bleeding.
Symptoms range from mild to severe. Common signs include:
Seek a doctor's help immediately if you notice:
Von Willebrand disease is usually inherited. Causes include:
You may be more likely to have von Willebrand disease if you:
Inherited von Willebrand disease cannot be prevented. However, bleeding episodes can be reduced by:
Von Willebrand disease is divided into three main types based on how much von Willebrand factor is in the blood and how well it works:
This is the most common and mildest form. About 3 out of 4 people with the disease have Type 1. The body produces less von Willebrand factor than normal. Bleeding is usually mild.
In this type, the body makes the protein, however it does not work properly. There are several subtypes such as 2A, 2B, 2M, and 2N. Bleeding is usually moderate.
This is the most severe and rarest form. The body produces very little or no von Willebrand factor. People with Type 3 can have heavy bleeding into joints and muscles, similar to hemophilia.
This form is not inherited. It develops later in life due to other medical conditions such as certain cancers, autoimmune diseases, or heart valve problems.
Doctors use a combination of tests to diagnose von Willebrand disease:
Treatment depends on the type and severity. The goal is to prevent and control bleeding while keeping a normal lifestyle.
(Home care supports medical treatment but cannot replace it. Always work with a hematologist.)
(All medicines must be selected by a hematologist.)
If not managed properly, von Willebrand disease can lead to:
Von Willebrand disease is best managed by a specialist. Marham helps you connect with trusted, verified, and experienced hematologists, gynecologists, and general physicians who can guide your treatment and family planning. Book an appointment with the best hematologist through Marham today.
Marham shares expert-reviewed information to support your health journey. The information on this page is only to guide and inform you. For any personal advice, it’s always best to check with a medical professional.
No. Both are bleeding disorders, however they involve different clotting factors. Von Willebrand disease affects the von Willebrand factor protein, while hemophilia involves factors VIII or IX. Von Willebrand disease is also far more common than hemophilia.
There is no cure for inherited von Willebrand disease, however bleeding can be well controlled with medicines, lifestyle care, and pre-treatment before surgery. Most people live full, active lives.
Most cases follow an autosomal dominant pattern, which means a person needs only one changed gene from one parent. Type 3 is autosomal recessive, where both parents must pass the changed gene to the child.
Both sexes are affected equally, however women notice symptoms more because of heavy menstrual bleeding and bleeding during childbirth. This makes the disease more likely to be diagnosed in women.
Pregnancy can be safe with proper planning. Von Willebrand factor levels usually rise during pregnancy. However, women still need careful monitoring and pre-delivery planning with a hematologist and gynecologist.
A hematologist (blood specialist) is the main doctor for this condition. Major hospitals in Pakistan have hematology services, and Marham can help you find a qualified specialist near you.