PPT-SICKLE CELL ANEMIA JASON ABOUDI MOUABBI MD

What is the most common genetic disorder in the United States Background Inheritance Pathophysiology Diagnostic testing Prognosis Management of acute illness Longterm management Treatment options. b. d. g. a. a. Chromosome 16. Chromosome 11. 25%. 25%. a. a. b. d. g. 25%. 25%. 48%. 48%. 1.5%. 0.5%. 1.5%. 0.5%. Hemoglobin synthesis. a. a. a. a. a. a. b. g. d. b. d. g. HbA. HbF. HbA. 2. 98%. ~1%. Jenny Pham. Protein Structure & Function. Spring 2015. Outline. Normal Adult Hemoglobin (. Hb. A). Function: Deoxygenated v. Oxygenated. Mutation in . Hb. A. Sickle Cell Hemoglobin (. Hb. S). Sickle Cell Anemia. was developed to create a greater awareness in . the Nashville . community of Sickle Cell Disease and to raise . funds for . patient care, . social services. , and research. . All . proceeds from the event . Presenter: Bridget H. Wilson, Ph.D., MS, RN. Introduction. Sickle cell disease (SCD) pain continues to emerge among adolescents. Over 98,000 individuals are believed to have SCD within the United States. . Katie Coltharp and Mariela Saenz. Names of Disorder. HbS. disease. Hemoglobin S disease. Hemoglobin SS disease. Sickling. disorder due to hemoglobin S. Sickle cell disease (broad term). Sickle cell disorders (broad group of conditions). the Emergency Physician and Nurse. Sickle Cell Pain. Carlton Haywood Jr., . PhD, . MA. Core . Faculty, the Johns Hopkins Berman Institute of Bioethics. Assistant Professor, The Johns Hopkins School of Medicine. Gary Strokosch, MD. Jane Litvin, MS. Introduction. History of . sickle cell disease . (SCD). Present in Africa for at least . 5,000. . years. 1910-. . Discovered in US. Walter Clement Noel – dental student from Grenada studying in Chicago. . Presenter: Bridget H. Wilson, Ph.D., MS, RN. Introduction. Sickle cell disease (SCD) pain continues to emerge among adolescents. Over 98,000 individuals are believed to have SCD within the United States. . the Emergency Physician and Nurse. Epidemiology, Genetics, Pathophysiology. . Paula Tanabe. , PhD, RN, FAEN, FAAN. Associate Professor. Duke University, Schools of Nursing and Medicine. Objectives. April 24, 2017. What is SSD?. SSD is an autosomal recessive disorder of a point mutation in the beta globulin chain in hemoglobin.. SSD is an autosomal recessive disorder of a point mutation in the beta globulin chain in hemoglobin.. Dr. Soheila . zareifar. Department of pediatric hematology/oncology. Shiraz university of medical sciences. Qeshm. 2018. Transfusion in Sickle Cell. In sickle cell disease transfusions improve blood flow by reducing the proportion of red cells capable of forming sickle hemoglobin polymer. . a sign . of an underlying . disorder. There are several kinds of anemia. . A. . physiologic . approach classifies anemia according to whether. the deficiency in erythrocytes is caused by a defect in . Susan E. Kirk, MSPAS, PA-C. Instructor, Baylor College of Medicine. Texas Children’s Hematology Center. April 15, 2016. Texas Children’s Hospital Advanced Practice Provider Conference. Disclosures. Abeer. . Anwer. Ahmed. Sickle cell disease is a group of . haemoglobin. disorders . resulting from . the inheritance of the sickle β‐. globin. gene. . Sickle cell disease (SCD) is . an. . autosomal.