Blank Is A Genetic Clotting Disorder.
Children born with a genetic clotting disorder are at a higher risk for developing blood clots. These inherited clotting disorders are usually caused by a deficiency in clotting factors or a genetic mutation, such as Factor V Leiden mutation, which affects 5% of people. Other common inherited clotting disorders include Von Willebrand's disease and hemophilia. These disorders can increase the risk of abnormal blood clots forming, commonly in the legs or lungs. Inherited clotting disorders can be diagnosed through genetic counseling and treatment may involve managing the underlying condition or prescription of medication.
A genetic clotting disorder refers to a condition where the blood's ability to clot properly is affected due to genetic factors. Some examples of genetic clotting disorders include Factor V Leiden mutation, Von Willebrand's disease, and hemophilia. These conditions can increase the risk of abnormal blood clot formation, which can lead to various health complications. Diagnosis typically involves genetic counseling and treatment may include managing the underlying condition or medication. If you have specific concerns about a genetic clotting disorder, it's best to consult with a healthcare professional for personalized guidance.
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