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What is Aplastic?

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What is Aplastic?

/ (eɪˈplæstɪk) / adjective. relating to or characterized by aplasia. failing to develop into new tissue; defective in the regeneration of tissue, as of blood cellsaplastic anaemia.

What is Animick?

Anemia is a condition in which you lack enough healthy red blood cells to carry adequate oxygen to your body’s tissues. Having anemia, also referred to as low hemoglobin, can make you feel tired and weak.

What deficiency causes clotting disorders?

Protein S deficiency is a disorder of blood clotting. People with this condition have an increased risk of developing abnormal blood clots. Individuals with mild protein S deficiency are at risk of a type of clot called a deep vein thrombosis (DVT) that occurs in the deep veins of the arms or legs.

What is coagulation deficiency?

Coagulation disorders are disruptions in the body’s ability to control blood clotting. Coagulation disorders can result in either a hemorrhage (too little clotting that causes an increased risk of bleeding) or thrombosis (too much clotting that causes blood clots to obstruct blood flow).

What is the meaning of the aplasia?

Aplasia is a condition in which an organ, limb, or other body part does not develop. In most cases, aplasia is obvious at birth.

What is anemia meaning?

Anemia occurs when there are not enough healthy red blood cells to carry oxygen to your body’s organs. As a result, it’s common to feel cold and symptoms of tiredness or weakness. There are many different types of anemia, but the most common type is iron-deficiency anemia.

What does a high hematocrit mean?

If your hematocrit is high, it means that you have more red blood cells than is considered healthy. High hematocrit may be caused by [4:1]: Heart disease. Dehydration. Scarring or thickening of the lungs.

What is protein S deficiency?

Protein S deficiency is a rare genetic disorder of blood coagulation that is caused by a variation in the PROS1 gene. This variation is inherited in an autosomal dominant manner.

Is antithrombin 3 deficiency hereditary?

Hereditary antithrombin deficiency is inherited as an autosomal dominant condition. Dominant genetic disorders occur when only a single copy of an altered gene is necessary for the appearance of the disease.

What is blood clotting disorder called?

The tendency… An excessive clotting disorder, also known as a hypercoagulable disorder or thrombophilia, is the tendency of some people to develop blood clots in parts of the body, such as the deep veins in the legs (called venous thromboembolism or DVT) or the arteries of the heart (arterial thrombosis).

What are the clotting disorders?

Large blood clots that do not break down can cause serious health problems.

  • Deep Vein Thrombosis (DVT)
  • Pulmonary Embolism (PE)
  • Arterial Thrombosis.
  • Antiphospholipid Antibody Syndrome (APLS)
  • Factor V Leiden.
  • Prothrombin Gene Mutation.
  • Protein C Deficiency, Protein S Deficiency, ATIII Deficiency.