'Beta thalassemia' presentation slideshows

HEMOGLOBINOPATHIES: Thalassemia and Sickle Cell (with brief mention of a few others)

HEMOGLOBINOPATHIES: Thalassemia and Sickle Cell (with brief mention of a few others). Peter Newburger, MD Departments of Pediatrics and Cancer Biology. Epidemiology and the malaria hypothesis.

1.62k views • 56 slides

U.S. Food and Drug Administration

720 views • 48 slides

What Is Thalassemia ?

What Is Thalassemia ?. Thalassemia is a group of inherited disorders of hemoglobin synthesis characterized by a reduced or absent output of one or more of the globin chains of adult hemoglobin .

1.05k views • 47 slides

Thalassemias

Thalassemias. Hemoglobin A. ?. ?. Fetal Hemoglobin (2 alpha, 2 gamma) Hemoglobin A2 (2 alpha, 2 delta) Small amounts in body. ?. ?. Disorders of Haemoglobin. 1. Thalassemia 2. Haemoglobinopathies. What is Thalassaemia ?.

600 views • 44 slides

Hemosiderosis

1.12k views • 40 slides

Plot The Clot

494 views • 32 slides

HEMOGLOBIN

HEMOGLOBIN. Heme is the prosthetic group of hemoglobin, myoglobin, & cytochromes MVMVMPPM. Structure of Heme. Normal Hemoglobin. HEME-CONTAINING PROTEINS ? Hemoglobin ? Myoglobin ? Cytochromes ? Catalase ? Some peroxidases. Synthesis of Hemoglobin. GLYCINE + SuccinylCoA.

830 views • 31 slides

Alterations of Hematologic Function in Children

Alterations of Hematologic Function in Children. Chapter 28. Fetal and Neonatal Hematopoiesis. The embryo becomes too large for oxygenation by simple diffusion Erythropoiesis begins within the vessels of the yolk sac

429 views • 27 slides

Presented to: Dr Lesley Johnson Human disease=Beta Thalassemia

Presented to: Dr Lesley Johnson Human disease=Beta Thalassemia. Presenter Name: Khazeema Yousaf 12-10308. By PresenterMedia.com. Summary Layout. Facts and theories. Types of Thalassemia. What causes which type? What is hemoglobin(structure)?Basic idea.

465 views • 20 slides

THALASSEMIA

Date of Presentation: September 23 rd , 2014 Date of Sign-up: September 9 th , 2014 Instructor: Dr. Jeffrey Henderson. THALASSEMIA. Chia-En Joanne Chang Amanda Chow Ju Pan (Harmony) Hsieh Linda Xi Yang. What Is thalassemia?.

6.18k views • 19 slides

Managing Iron Overload in Beta Thalassemia Major: Focus on Cardiac Iron

Managing Iron Overload in Beta Thalassemia Major: Focus on Cardiac Iron. Ali Taher, MD American University of Beirut Lebanon. Baseline Patient Characteristics. At presentation 22-year-old male patient diagnosed with beta thalassemia major at age 6 months Normal ECG

1.3k views • 18 slides

OSPE FILE (HAEMATOLOGY)

OSPE FILE (HAEMATOLOGY). Notes:. Each single word in this file is important especially the findings You have to write them all even the normal! You have to write the word DISEASE in the cases of sickle cells anemia to differentiate it from sickle cell trait

597 views • 18 slides

Chapter 7

228 views • 13 slides

Thalassemia & Treatment

PHM 226, Example Instructor: Dr. Jeffrey Henderson. Thalassemia & Treatment. Genetic disruption of the synthesis of hemoglobin Victor Wong ( victorwong@rogers.com ) Tracy Wong ( bigmama27@hotmail.com ) Bao Nguyen ( bao.nguyen@utoronto.ca ) PHM 226 January 13 th , 2003.

369 views • 13 slides

Thyrocare - Diagnostic Lab in Shalimar Bagh, Delhi | Lybrate

Thyrocare is a diagnostic lab in Shalimar Bagh, Delhi. View details tests costs, labs timings, address and contact labs directly on Lybrate.com | Lybrate

77 views • 5 slides

alpha thalassemia Market

The alpha thalassemia is segmented on the basis of type, diagnosis, treatment, and end-users.

53 views • 3 slides

Alpha Thalassemia Market Research 2019

Alpha Thalassemia Market Research Report - Global Forecast Till 2023

40 views • 3 slides