Affected individuals also have a shortage of red blood cells anemia, which can cause pale skin. Your body makes less of the beta chains, but is still able to make plenty of. Beta thalassemia trait when you have one working copy of the beta globin gene and one nonworking copy you have beta thalassemia trait. Medlineplus en espanol tambien contiene enlaces a sitios web no gubernamentales. Talasemias hematologia y oncologia manual msd version. Talasemias hematologia y oncologia manual merck version. Create marketing content that resonates with prezi video. Dna contains both the instructions for stringing amino acids together into proteins, as well as stretches of dna that play important roles in regulating produced protein. Beta thalassemia is a blood disorder that reduces the production of hemoglobin. In beta thalassemia, the gene for making beta globin chains doesnt work normally. Beta thalassemia trait and beta thalassemia disease. Aehh balcells 2125, bajos, local 1 08024 barcelona tfno 93 285 75 55. To determine the frequencies of betathalassemia mutations in different states of india and to compare this with the available data in asian indians for a comprehensive.
Hemoglobin is the ironcontaining protein in red blood cells that carries oxygen to cells throughout the body. Beta thalassemia is a hereditary disease affecting hemoglobin. As with about half of all hereditary diseases, an inherited mutation damages the assembly of the messengertype rna mrna that is transcribed from a chromosome. Dna contains both the instructions genes for stringing amino acids together into proteins, as well as stretches of dna. Delta betatalasemia anemias minoritarias catglobin. In people with beta thalassemia, low levels of hemoglobin lead to a lack of oxygen in many parts of the body.
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