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Thalassemia and Genetics: What You Need to Know

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  Thalassemia is a genetic blood disorder that affects the body’s ability to produce hemoglobin, an essential protein in red blood cells. Hemoglobin is responsible for carrying oxygen throughout the body. When the body doesn’t produce enough of it, it leads to anemia, fatigue, and other health complications. Thalassemia is inherited from parents, which means it’s passed down through genes. If both parents carry the thalassemia gene, there’s a higher chance their child will be born with the disorder. There are two main types: alpha thalassemia and beta thalassemia, with the latter being more severe. Depending on how many genes are affected, the severity of symptoms can vary, ranging from mild anemia to life-threatening conditions that require regular blood transfusions. If you or your child is diagnosed with thalassemia, it's crucial to consult with a hematologist in Noida for proper guidance and treatment. Regular monitoring and specialized care are essential in managing the sympt

Anemia Causes, Symptoms, Diagnosis, and Other Facts

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Anemia is a condition where your body doesn't have enough healthy red blood cells to carry oxygen to tissues, making you feel tired and weak. It can be caused by various factors, ranging from nutritional deficiencies to chronic diseases. Read more: https://medium.com/@drpawankumarsingh8/anemia-causes-symptoms-diagnosis-and-other-facts-40393ce1d0b0