Correct trait in AFP smoothly

Aug 6th, 2022
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How to Correct trait in AFP

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hello everyone and welcome to the channel in todays video Raphael Advanced defense systems limited showcased the impressive Firepower of the Philippine Navys newest asset the shaldeg MKV missile boats typhoon MK 30C turret the naval gun was put to the test in a firing exercise aimed at an unmanned aerial vehicle or UAV and the results were remarkable as we can see in the footage the typhoon mk30c successfully destroyed the UAV demonstrating its Superior ship perimeter protection and high level of stabilization and pointing accuracy the typhoon mk-30c is the newest member of the typhoon family of stabilized Naval rcws which is designed to counter emerging aerial and asymmetric swarm attack threats the naval gun uses the mk-44 bushmaster gun and is fully compatible with high explosive and air burst ammunition or ABM using a single ammunition load the typhoon mk-30c can defeat multiple small and medium uas including the latest emerging drone threats the naval gun uses the mk-44 bushmas

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A person who has thalassemia trait may not have any symptoms at all or may have only mild anemia, while a person with thalassemia major may have severe symptoms and may need regular blood transfusions.
When thalassemia is called alpha or beta, this refers to the part of hemoglobin that isnt being made. If either the alpha or beta part is not made, there arent enough building blocks to make normal amounts of hemoglobin. Low alpha is called alpha thalassemia. Low beta is called beta thalassemia.
What is alpha thalassemia? Alpha thalassemia is a condition which affects the hemoglobin in the blood. Hemoglobin is the part of the red blood cells that carries oxygen through the body. Alpha thalassemia is found most often in people of Asian origin, but it also regularly appears in people of African ancestry.
All 4 genes are missing. This causes severe anemia. In most cases, a baby with this condition will die before birth.
Alpha thalassemia is an inherited blood disorder in which the body doesnt make as much alpha globin. Alpha globin is a building block of hemoglobin. Hemoglobin is the part of red blood cell (RBC) that carries oxygen throughout the body.
There are 4 types of alpha thalassemia: Alpha thalassemia silent carrier. One gene is missing or damaged, and the other 3 are normal. Blood tests are usually normal. Alpha thalassemia carrier. Two genes are missing. Hemoglobin H disease. Three genes are missing. Alpha thalassemia major. All 4 genes are missing.
Laboratory diagnosis of -thalassemia requires molecular analysis for the confirmatory diagnosis. A screening test, comprising complete blood count, blood smear and hemoglobin quantification by high performance liquid chromatography and capillary electrophoresis, may not possibly detect all the thalassemia diseases.
In people with the characteristic features of alpha thalassemia, a reduction in the amount of hemoglobin prevents enough oxygen from docHubing the bodys tissues. Affected individuals also have a shortage of red blood cells (anemia ), which can cause pale skin, weakness, fatigue, and more serious complications.

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