PPT-THALASSEMIA Dr. M. A. SOFI

MD FRCP London FRCPEdin FRCSEdin T halassemia Hemoglobin molecule is the ironcontaining oxygentransport metalloprotein in the red blood cells of all vertebrates The normal haemoglobin. Ashutosh Lal, MD. Northern California Thalassemia Center. UCSF Benioff Children’s Hospital Oakland. Thalassemia Syndromes: . Many diagnoses. Oakland Data (n=203). What is the proportion of . non-transfusion-dependent thalassemia. C TAGALOG Ano ang Thalassemia?ng Thalassemia ay isang uri ng makakuha ng sapat na oxygen ang dugo, atTaon-taon ay dumarami ang bilang ngmga sanggol na ipinapanganak na mayAno ang mga palatandaan ngMay C TAGALOG Ano ang Thalassemia?ng Thalassemia ay isang uri ng makakuha ng sapat na oxygen ang dugo, atTaon-taon ay dumarami ang bilang ngmga sanggol na ipinapanganak na mayAno ang mga palatandaan ngMay 1 Terms and Conditions Apply. SOFI RESERVES THE RIGHT TO MODIFY OR DISCONTINUE PRODUCTS AND BENEFITS AT ANY TIME WITHOUT NOTICE. To qualify, a borrower must be a U.S. citizen or permanent resident i SimplicityRefinanceandconsolidateallstudentloans(bothfederalandprivate) intosingloanwithonemonthlypayment.No Feesapplicationfeesorigination feesprepaymentpenalties,disbmentfeesTheapplicationprocesssim How to apply: Find your rates at:If approved, select your rate and termUpload identity, income and loan information *Terms and Conditions Apply. SOFI RESERVES THE RIGHT TO MODIFY OR DISCONTIN How to apply: Find your rates at:If approved, select your rate and termUpload identity, income and loan information *Terms and Conditions Apply. SOFI RESERVES THE RIGHT TO MODIFY OR DISCONTIN Welcome Bonus: AllCHOCassociates, family members and friends are eligiblefor a0.125% rate discountthrough sofi.com/choc. Applicants mustapply through the sofi.com/choc link to qualify for the rate 1Terms and Conditions Apply SOFI RESERVES THE RIGHT TO MODIFY OR DISCONTINUEPRODUCTS AND BENEFITS AT ANY TIME WITHOUT NOTICE To qualify a borrower must be aUS citizen or permanent resident in an eligi Thalassemia . is an inherited blood disorder in which the body makes an abnormal form of hemoglobin. Hemoglobin is the protein molecule in red blood cells that carries oxygen. Hemoglobin is formed by the combination of . : are genetic(AR) disorders in . globin. chain production. . In individuals with β. -thalassemia. , there is either: . complete. absence of β-globin gene production . (β. 0. -thalassemia). Kakavoulis. . Nikolaos. Patras Ioannis. What is . Thalassaemia. ?. . Thalassaemia. is a group of inherited disorders of hemoglobin synthesis characterized by . reduced . or . absen. ce. . of one . Silent carrier . α. -/. αα. . Normal complete blood count . α. -Thalassemia trait . αα. /- - (. α. -thalassemia 1) . or . α . -/. α . - (. α. -thalassemia 2) . Mild microcytic anemia . Hemoglobin H . DEFINITION: . Thalassemia is blood disorder passed down through families (inherited) in which the body makes an abnormal form or inadequate amount of . haemoglobin. .. CAUSE:. . Haemoglobin. made of 2 proteins: .