
Hemophilia Treatment in Dubai at Emirates Hospitals Group. We are dedicated to providing comprehensive, specialized care for patients with Hemophilia, a rare but serious bleeding disorder. Our expert team of hematologists is well-versed in the diagnosis and management of this condition, ensuring patients receive personalized care with the latest treatment options. We understand the challenges faced by individuals with hemophilia and are committed to improving their quality of life through effective, compassionate medical care.
Hemophilia is a genetic disorder that impairs the body’s ability to make blood clots, a process essential for stopping bleeding. It is caused by a deficiency in specific clotting factors—proteins in the blood that work together to form clots. The most common types of hemophilia are:
Hemophilia is typically inherited and primarily affects males, although females can be carriers and may exhibit mild symptoms. It is a lifelong condition, but with modern treatments and comprehensive care, individuals with hemophilia can lead healthy and active lives.
The severity of hemophilia is classified based on the level of clotting factors in the blood:
The primary symptom of hemophilia is prolonged or spontaneous bleeding, which can occur internally (inside joints and muscles) or externally (from cuts or injuries). Key symptoms include:
Causes of Hemophilia are primarily genetic. It is an X-linked recessive disorder, meaning the gene causing hemophilia is located on the X chromosome. Since males have only one X chromosome, a single altered gene is sufficient to cause the condition. Females, with two X chromosomes, are typically carriers and may only show mild symptoms if one of their X chromosomes carries the mutated gene.
In rare cases, hemophilia can develop later in life (acquired hemophilia) due to autoimmune diseases, cancers, or complications from certain medications.
At Emirates Hospitals Group, we offer a comprehensive approach to managing hemophilia, utilizing the latest therapies to prevent and treat bleeding episodes. The primary goal of treatment is to replace the missing clotting factors and manage symptoms effectively.
Hemophilia is a genetic disorder where the blood does not clot properly due to a deficiency in clotting factors, leading to excessive or spontaneous bleeding.
Diagnosis involves a series of blood tests, including a clotting factor assay, which measures the levels of specific clotting factors to determine the type and severity of hemophilia.
While there is currently no cure for hemophilia, treatments like clotting factor replacement therapy and emerging gene therapies can effectively manage symptoms and improve quality of life.
High-impact sports and activities with a risk of injury should be avoided. However, with proper treatment and precautions, many patients can engage in safe exercises and activities.
Hemophilia primarily affects males, but women can be carriers of the gene. Female carriers may experience mild symptoms and should seek medical advice if they show signs of a bleeding disorder.
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