PPT-Sickle cell anaemia Ass. Prof.

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. 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. PALI Haematology Session. 3. rd. October 2012. Christopher Mullen. Introduction. Classification. The Hypochromic . Anaemias. Megaloblastic. and other macrocytic . anaemias. Haemolytic . anaemias. Genetic disorders of haemoglobin. Patterns of inheritance. Learning outcomes. (. i. ) . genetic diagrams to show patterns of . inheritance. To . include monogenic inheritance, dihybrid inheritance. , multiple alleles, sex linkage. and codominance.. What do you mean by variation..?. Differences between species. Differences within a species. SPECIES : . A . species.  is a group of organisms that are able to interbreed and produce . fertile.  offspring.. MBBS, DMU, MD, PhD. Associate Professor, Cardiology. College of Medicine, ALJOUF University, KSA. Outlines. HAEMOLYTIC ANAEMIA. APLASTIC ANAEMIA . SICKLE-CELL ANAEMIA . HAEMOLYTIC ANAEMIA. Haemolytic Anaemia . . Sickle cell is a red blood disorder that can cause red blood cell to change form and cause lots of pain. Unfortunately this disorder can not be cured but can be stabled with the right treatments. In 1973 the average lifespan of a person with sickle cell was only 14 years. Ass. Prof. . Abeer. . Anwer. Ahmed. Sickle cell . anaemia. Ass. Prof. . Abeer. . Anwer. Ahmed. Sickle cell disease is a group of . haemoglobin. disorders . resulting from . the inheritance of the sickle β‐. . . Abeer. . Anwer. Ahmed. Pallor of the . conjunctival. mucosa . in patient . with severe . anaemia. Koilonychia - spoon shaped nail. Blood film of IDA. : . Hypochromic. . microcytic. RBCs with . Anaemia . Decreased Hb level. Male . Female . RBC count (million/. μ. l). 4.5-6. 4-5. Haemoglobin level (g/dl). 13-16. 12-15. Hematocrit. %. 40-50. 35-45. Normal values for Hb, RBC count, hematocrit . (2) to work to ensure that adequate, appropriate and accessible emergency care is available to persons living with sickle-cell anaemia; to develop their capacity to evaluate the situation regarding si Disease Education 5/17 Care of patients with sickle cell disease for primary care providers and emergency room personnel Table of Contents Chapter 1: Background About Sickle Cell Disease and Making t October 11, 2023. Jennifer Colozza, PharmD. Clinical Pharmacist. MO HealthNet Division. During . at least one regularly scheduled meeting each calendar year, the advisory council on rare diseases and personalized . comms toolkit. What is the campaign?. Overview . NHS England and NHS Improvement is continuing it’s Sickle Cell awareness campaign ahead of World Sickle Cell Day 2023.. Objectives/Aims. The campaign, which is part of a bigger drive to improve sickle cell care across the NHS, aims to increase awareness of the key signs and symptoms of a Sickle Cell crisis, particularly among urgent emergency care staff and those living with the condition and their carers.. Dr.Maysem. M. . Alwash. Sickle cell . disaese. Sickle cell disease (SCD) is an inherited chronic . haemolytic. . anaemia. . whose clinical manifestations arise from the tendency. of the . haemoglobin.