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What are Bleeding Disorders

Introduction

Bleeding disorders are uncommon conditions that impair how the body regulates blood coagulation. If your blood does not clot normally, you may have problems with excessive bleeding after an injury or surgery. This health issue will concentrate on bleeding disorders caused by clotting factor deficiencies, such as hemophilia and von Willebrand disease.

Clotting factors, also known as coagulation factors, are proteins found in the blood that collaborate with small cells known as platelets to produce blood clots. A bleeding condition can result from any problem that affects the function or amount of clotting factors or platelets.

A bleeding disease can be hereditary, which means you were born with it, or acquired, which means it developed later in life. Symptoms include easy bruising, heavy menstrual cycles, and frequent nosebleeds. To diagnose a bleeding condition, your doctor will examine your symptoms, risk factors, medical history, and blood test findings.

Types of Bleeding Issues

To address the bleeding issue, your doctor may prescribe medications or clotting factor replacement treatment. Some bleeding issues are chronic, and others might lead to consequences. Even if you do not require medication to treat the bleeding disease, your doctor may advise you to take precautions before a medical operation or during a pregnancy to avoid future bleeding problems.

Bleeding disorders can be hereditary or acquired, which means they develop over your lifetime. Inherited bleeding diseases are less prevalent than acquired bleeding disorders.

Disorders of acquired hemorrhage

A bleeding problem can occur if anything in your body, such as a disease or medication, causes your body to cease producing blood clotting factors or causes the blood clotting factors to stop acting properly. Furthermore, problems with your blood arteries can result in bleeding.

Among the acquired bleeding diseases are:

  • Intravascular coagulation that has spread (DIC)
  • Vitamin K deficiency bleeding Von Willebrand disease and hemophilia, which are most commonly inherited but can arise as a result of a medical issue
  • Other, less common types of acquired bleeding disorders include deficits in specific factors, such as factor I, II, and V, which are called after the clotting factor that is causing the problem.
  • Arteriovenous malformations are rare tangles of blood vessels that can occur in the brain or elsewhere in the body and cause bleeding before birth or later in life.

Bleeding diseases that are inherited

Among the inherited bleeding diseases are:

  • Hemophilia C is a rare condition also known as factor XI deficiency Von Willebrand disease (VWD), which has multiple categories that are numbered based on how common the condition is and how severe the symptoms are.
  • Hemophilia B is caused by a lack of clotting factor IX or by having low amounts of clotting factor IX.
  • Combined shortage of vitamin K-dependent clotting factors (VKCFDs), produced by clotting factor II, VII, IX, and X problems.
  • Hemophilia A, the most prevalent kind of hemophilia, is caused by a lack of or low amounts of clotting factor VIII.
    Other hereditary bleeding diseases include rare bleeding disorders such as I, II, V, V + VIII, VII, X, XI, or XIII deficits, which are called after the clotting factor that causes the condition. deficits in other factors
    Hereditary hemorrhagic telangiectasia is a rare genetic disorder characterized by twisted blood arteries in many regions of the body that can result in bleeding.

Conclusion

We have been able to see here that Vitamin K deficiency bleeding Von Willebrand disease and hemophilia, which are most commonly inherited but can arise as a result of a medical issue. If you have any questions or concerns about what is written here please comment in the discussion below. contact us Rovich Diagnostic Services for consultancy.

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