'Thalassemia' diaporamas de présentation

Thalassemia and Hemoglobinopathies

Thalassemia and Hemoglobinopathies. Ahmad Shihada Silmi Msc, FIBMS Staff Specialist in Hematology Medical Technology Department Islamic University of Gaza. Quiz. What is structure of hemoglobin A? What is the normal hemoglobin types in normal adults?

2.06k views • 131 slides

Hematological disorders in pregnancy

5.38k views • 83 slides

Allogeneic Hematopoietic Stem Cell Transplant in Severe Thalassemia Patients: Time to Transplant

Allogeneic Hematopoietic Stem Cell Transplant in Severe Thalassemia Patients: Time to Transplant. Suradej Hongeng, MD Professor of Pediatrics Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand. Outline. Definition of severe thalassemia

1.08k views • 80 slides

Allogeneic Hematopoietic Stem Cell Transplant in Severe Thalassemia Patients: Time to Transplant

Allogeneic Hematopoietic Stem Cell Transplant in Severe Thalassemia Patients: Time to Transplant. Suradej Hongeng, MD Professor of Pediatrics Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand. Outline. Definition of severe thalassemia

1.27k views • 80 slides

Stem Cells

Stem Cells. Embryonic stem cells Adult (Somatic) stem cells. ES cells line. Pluripotentiality property Immortal property. Nucleus transfer. Fusion of somatic cells and embryonic cells. Embryonic stem cell (ES) Endoderm Mesoderm Ectoderm Germ cell line

833 views • 60 slides

Prof. Mervat Hesham 2010

Prof. Mervat Hesham 2010. Hemoglobinopathies. Definition of Anemia. Decrease in Hgb. Decrease in rbc decrease in hct below the normal for the age and sex. Different ways to classify anemia. *Mechanism of its production *Size and hemoglobin content of rbc.

1.01k views • 58 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

THALASSEMIA : A DREADFUL DISEASE TURNED TO A CHRONIC CONDITION Dimitris Loukopoulos, MD

THALASSEMIA : A DREADFUL DISEASE TURNED TO A CHRONIC CONDITION Dimitris Loukopoulos, MD University of Athens, Greece. A lecture dedicated to the late Professor Antonio CAO (+2012). Thalassemia.

519 views • 34 slides

Hematology 425 Thalassemias

Hematology 425 Thalassemias. Russ Morrison November 17, 2006. Thalassemias. Thalassemias are a diverse group of inherited disorders caused by gene mutations These gene mutations reduce or completely eliminate the synthesis of one or more of the globin chains of the Hgb tetramer

472 views • 32 slides

SENSITISATION PROGRAMME FOR CENSUS ENUMERATORS ON DISABILITY QUESTION IN CENSUS 2011

434 views • 29 slides

Hemoglobinopathies

995 views • 29 slides

Thalassemia and Hemoglobinopathies

1.87k views • 27 slides

GENETIC BACKGROUND IN THALASSEMIA

426 views • 24 slides

Hemolytic anemias - Hemoglobinopathies

Hemolytic anemias - Hemoglobinopathies. Part 2. Thalassemias. Thalassemias are a heterogenous group of genetic disorders Individuals with homozygous forms are severely affected and die early in childhood without treatment Heterozygous individuals exhibit varying levels of severity

719 views • 19 slides

FOLLOW UP IN THALASSEMIA CLINIC

FOLLOW UP IN THALASSEMIA CLINIC. Presented by: Dr. Afsana Jahan (PGT) Dr. Aditi Baruah (MD); Dr. P. Bishwanath (MD) Department of Paediatrics Assam Medical College & Hospital, Dibrugarh. Introduction.

456 views • 19 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

thalassemia

p. thalassemia. Pathophysiology.

586 views • 18 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

DNA & Mutations

232 views • 11 slides