PPT-THALASSEMIA MINOR DIAGNOSTICS

BY A COMPUTATIONAL METHOD Yulia Einav Holon Institute of Technology Israel Outline Introduction Sys tem desi g n Results Summary amp Conclusions Acknowledgements α and β thalassemia are the most common . Ellis J. Neufeld MD, PhD. Egan Family Foundation Chair in Transitional Medicine, Harvard Medical School. Associate Chief, Dana-Farber Boston Children’s Center for . Cancer and Blood Disorders . Chair, Medical Advisory Board, CAF. 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. J. Komppula. &. JYFL . ion source . group. University of . Jyväskylä. Department . of . Physics. Finland. Motivation. Diagnostics challenging. Experimental plasma parameters. R. i. . =. . n. e. 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 The global molecular diagnostics market was worth USD 15.29 billion in 2020 and is further projected to reach USD 31.98 billion by 2027, at a CAGR of 11.1% during the forecast period (2021-2027). The global molecular diagnostics market was worth USD 15.29 billion in 2020 and is further projected to reach USD 31.98 billion by 2027, at a CAGR of 11.1% during the forecast period (2021-2027). ACCESS INITIATIVE to achieve the 90-90-90 treatment target2 DIAGNOSTICS ACCESS INITIATIVE to achieve the 90-90-90 treatment targetBACKGROUNDA new target for HIV treatment scale-up31e world is uniting MD; FRCP (London); . FRCPEdin. ; . FRCSEdin. T. halassemia. Hemoglobin molecule. : is the iron-containing oxygen-transport . metalloprotein. in the red blood cells of all vertebrates.. The normal . haemoglobin. 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: .