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Thalassemia (thal-uh-SEE-me-uh) is a blood disorder. It's inherited, BloodVitals SPO2 which suggests it's handed from mother and BloodVitals SPO2 father to children through genes. Genes carry data that can affect many issues, including what individuals seem like and whether they might have sure diseases. Thalassemia causes the body to have much less of the protein hemoglobin than typical. Hemoglobin is current in pink blood oxygen monitor cells and permits the pink blood cells to hold oxygen. Not having sufficient hemoglobin or pink blood cells can lead to a situation called anemia. That can make you're feeling tired and Blood Vitals weak. When you've got a mild type of thalassemia called thalassemia trait, you do not want any particular treatment. But with extra-critical varieties, you might want common blood transfusions. Those are treatments by which you obtain blood from a donor. Lifestyle modifications also are key. For example, a wholesome food regimen and regular train can help you manage tiredness. There are various kinds of thalassemia. The symptoms that you've depend on the kind and how severe it's.

Tiredness, blood oxygen monitor also referred to as fatigue. A change in skin coloration or a yellowing of pores and skin and wireless blood oxygen check eyes. Changes or problems with facial bones. Swelling of the stomach area, additionally known as the abdomen. Some infants show signs of thalassemia at delivery. Others get signs during the primary two years of life. But some folks with thalassemia do not have symptoms. Make an appointment together with your kid's health care team for blood oxygen monitor a checkup in case your little one has any of the signs of thalassemia. We use the information you present to deliver you the content you requested. To give you the most relevant and blood oxygen monitor useful information, we may combine your electronic mail and website data with different data we have now about you. If you're a Mayo Clinic patient, we are going to solely use your protected health data as outlined in our Notice of Privacy Practices. Chances are you'll opt out of e mail communications at any time by clicking on the unsubscribe link in the e-mail.

Thalassemia is attributable to gene changes in cells that make hemoglobin. Hemoglobin is the protein in purple blood cells that carries oxygen all through the physique. The gene changes linked with thalassemia are handed from dad and mom to children. Hemoglobin molecules are made from protein chains called alpha and beta chains. These chains are affected by gene changes. With thalassemia, the physique does not make enough of either the alpha or the beta chains. That causes you to get both alpha-thalassemia or beta-thalassemia, the 2 important varieties of the situation. In beta-thalassemia, the gene change is an alteration in the DNA. Other terms used to describe these modifications embody mutation or variation. In alpha-thalassemia, the altered DNA consists of missing a number of copies of the four genes that program the alpha chain. With alpha-thalassemia, the seriousness of the condition is determined by the variety of lacking genes you inherit from your mother and father. The more missing copies of the genes, the worse your thalassemia.

With beta-thalassemia, blood oxygen monitor the seriousness of the situation relies on which part of the hemoglobin molecule is affected. Four genes are concerned in making the alpha hemoglobin chain. You get two from every of your parents. If one copy of the gene is missing, BloodVitals test you will haven't any symptoms of thalassemia. But you carry the illness and might cross it on to your children. If two copies of the genes are missing, your thalassemia symptoms possible will likely be mild. You might hear this condition known as alpha-thalassemia trait. If three copies of the genes are missing, your symptoms likely can be average to severe. It's uncommon to be missing all four copies of the genes. It often results in stillbirth. That is the loss of a pregnancy at or after 20 weeks. Babies born with 4 missing genes often die shortly after start. Or they want blood transfusions for the rest of their lives.

Sometimes, a baby born with this situation can be treated with blood transfusions and a stem cell transplant. Two genes are concerned in making the beta hemoglobin chain. You get one from every of your mother and father. Unlike the missing genes that cause alpha-thalassemia, small changes in the gene cause beta-thalassemia. These changes lead to decreased production of the beta chain. One gene with adjustments, you may often have mild symptoms. This situation is named nontransfusion-dependent thalassemia. If you don't have any signs, you could hear your condition called beta-thalassemia trait or thalassemia minor. Two genes with modifications, your signs typically can be average to extreme. This condition is named transfusion-dependent beta-thalassemia or blood oxygen monitor thalassemia main. Babies born with two changed beta hemoglobin genes often are healthy at beginning. They usually get symptoms inside the first two years of life. However it is possible to get a milder form of the disease with two modified genes. Family history of thalassemia.