Beta Thalassemia

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3- Hemoglobin H Disease • 1 functional globin gene • results in very lightly coloured red blood cells and possible severe anemia • hemoglobin H is susceptible to oxidation, therefore oxidant drugs and foods are avoided • treated with folate to aid blood cell production
4- Alpha <strong>Thalassemia</strong> Major or ( Hydrops Fetalis ) • no functional globin genes • death before birth (embryonic lethality)
Page 1 and 2: Genetics of Thalassemia Submitted b
Page 3 and 4: Thalassemia : oFirst recognized in
Page 5 and 6: Molecular Genetics : The genes that
Page 7 and 8: Sura Zuhair Salih • Types of Thal
Page 9 and 10: Alpha Thalassemia • mutation of 1
Page 11: 2- Alpha Thalassemia Trait • 2 fu
Page 15 and 16: Beta Thalassemia • mutations on c
Page 17 and 18: 2- Beta Thalassemia Intermedia •
Page 19 and 20: Pathophysiology of -Thalassemia/Hb
Page 21 and 22: Laboratory Diagnosis :
Page 23 and 24: Laboratory Diagnosis of Thalassaemi
Page 25 and 26: Laboratory Findings • Hb concentr
Page 27 and 28: Blood film in β-Thalassemia major
Page 29 and 30: 4- Hemoglobin Electrophoresis : Hem
Page 31 and 32: Sama Naal Salouha • Inheritance o
Page 33 and 34: Inheritance of Thalassemia : 1- If

Beta Thalassemia

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