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Is Gender A Factor In Thalassemia
No, but. . .: Environmental factors generally do not play a role in beta thalassemia. However, a patient can be worsened by conditions that typically worsen anemia, such as dietary iron deficiency, other nutrient deficiencies (such as folate (folic acid) or vitamin b12), lead poisoning, or infections with viruses that can cause anemia (such as parvovirus b19). Vacationing at high altitudes may cause symptoms of low oxygen. ...Read moreSee 1 more doctor answer
If a girl with G6PD want to marry someone with with thalasemia what are the risk factors of having kids? Is it bad?
My brother has Thalasemia, little liver sweeling.Recently 17mm gallstones has diagnosed.What will be the treatment and risk factors for him ?
Gallstone ? disease: Stones in the gallbladder (gb) seldom cause symptoms unless they migrate into the neck of the gb (& block exit of bile) or into the common bile duct. Symptomless gallstones may be diagnosed by chance by imaging or during investigation for some other condition. Only 10% become symptomatic within 5 years of detection. Ultrasound, ct scan, mrcp finds stones; cck-hida scan can tell if gb is diseased. ...Read moreSee 2 more doctor answers
Thalassemia: Thalassemia is a deficiency in the production of one of the globin chains (alpha or beta) that make up hemoglobin. Normally synthesis of these is balanced. When imbalanced, one globin accumulates relative to the other forming inclusions that are damaging to the red cells that contain them. There are many thal variants that manifest a wide severity of symptoms from none to transfusion dependence. ...Read moreSee 2 more doctor answers
Familial blood trait: Thalassemia runs in families. It is caused by variations (mutations) in DNA, which is then passed on to future generations. There are many variations in the DNA (genes) that code for hemoglobin molecules inside red blood cells. Some of these variations cause the hemoglobin production to be very slow, so blood cells stay too small because they can't form enough hemoglobin to grow to normal size. ...Read more
Millions of carriers: Thalassemia is one of the most common gene mutations in the world. Overall, an estimated 20-25 million people are carriers (1/300) (about 1/1000 in low-risk peoples, and about 1/30 in high-risk peoples). Low risk: japanese, korean, n. European caucasians, native canadians, native americans. High risk: mediterranean, middle eastern, south asian, south-east asian (western pacific rim), caribbean. ...Read moreSee 1 more doctor answer
From Mom and/or Dad: Alpha thalassemia is caused by a mutation in one or more of the 4 genes that code for (holds the dna for) Alpha globulin, which is needed to make hemoglobin for new red blood cells. Beta thalassemia is caused by a mutation in one or both of the 2 beta globulin genes. Mom and/or dad can carry the mutations. A child can inherit a mutation from mom, from dad, or from both mom and dad. ...Read moreSee 1 more doctor answer
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