PPT-Thalassemia Syndromes Thalassemias

are geneticAR disorders in globin chain production In individuals with β thalassemia there is either complete absence of βglobin gene production β 0 thalassemia. Fahd . Alareashi. .. . Anemia…. What is Anemia?. A condition characterized by a decrease in RBCs mass, hemoglobin or RBCs count.. Adult male: . Hb. .  13 g/. dL. , or . Hct. .: 41%.. Adult Females: . 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. Julie A. Dunlap, MS, CCC-SLP. SPHSC . 543. Winter 2010. Genetic Diseases. ~3-4% of all children are born with a major genetic or congenital disease . Not only extremely rare diseases. Importance of correct diagnosis. .. . Anemia…. What is Anemia?. A condition characterized by a decrease in RBCs mass, hemoglobin or RBCs count.. Adult male: . Hb. .  13 g/. dL. , or . Hct. .: 41%.. Adult Females: . Hb.  12 g/. Dr.Ayesha. . Junaid. MBBS,MCPS,FCPS.. Professor of Pathology. National . Hemovigilance. Coordinator . Supervisor & Program Director . Haematology. CPSP. Incharge. Blood transfusion services. Shifa. Thalassemia. Prof. Firoza Begum. High Risk Pregnancy & Infertility Specialist. Chairman, Fetomaternal Medicine . Dept. , BSMMU. Introduction. Hemoglobinopathies. are among the most common inherited diseases.. BY A COMPUTATIONAL METHOD. Yulia Einav. Holon Institute of Technology. Israel. Outline. Introduction. Sys. tem. desi. g. n. Results. Summary & Conclusions. Acknowledgements. α and β thalassemia are the most common . 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 . مؤيد . علو. ش. Lec. . 2. Thalassaemias. Objectives:. 1-Define thalassemia and its main types(. β. and . α. ). 2- Know the . genetic . lesions of each of . β . and . α. thalassemia. 3-Know the difference between thalassemia minor and major.. 1- what is the mode of inheritance in the vast majority f spherocytosis cases?. Autosomal dominant. Autosomal recessive. X-linked dominant. X linked recessive. 2- The amino acid present at the sixth position of the normal alpha-globin chain is replaced by which one of the following amino acids in sickle cell disease?. THALASSEMIA SYNDROMES Info Sheet 1800ROSWELL (1  8007679355) | RoswellPark.org UNDERSTANDING HEMOGLOBIN This important protein in your red blood cells carries oxygen PeeraponWongpeeraponw@nu.ac.thThalassemiaResearchUnit,FacultyofMedicine,NaresuanUniversity,99Moo9,TambonTahpoe,AmphurMuaeng,Phitsanulok65000,ThailandAnnHematolDOI10.1007/s00277-017-3089-4 Withthisfals F.I.B.M.S (Int. Medicine) , F.I.B.M.S (Hematology). DEFINITION. Thalassemias . are inherited blood disorders characterized by defect . in the rate of synthesis of one . of the . globin chains.. Resultant imbalance of globin chain production may cause ineffective . Dr . Tasneem. . Ara. . Associate Professor. Department of Hematology & Bone marrow transplantation unit . DMCH . 11/11/18. This presentation includes. Introduction. Social awareness . Screening for .