PPT-THALASSEMIA & HOMOEOPATHY
Author : Sunshine | Published Date : 2022-08-04
DEFINITION Thalassemia is blood disorder passed down through families inherited in which the body makes an abnormal form or inadequate amount of haemoglobin CAUSE
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THALASSEMIA & HOMOEOPATHY: Transcript
DEFINITION Thalassemia is blood disorder passed down through families inherited in which the body makes an abnormal form or inadequate amount of haemoglobin CAUSE Haemoglobin made of 2 proteins . Ashutosh Lal, MD. Northern California Thalassemia Center. UCSF Benioff Children’s Hospital Oakland. Thalassemia Syndromes: . Many diagnoses. Oakland Data (n=203). What is the proportion of . non-transfusion-dependent thalassemia. Dr . Meenal. . Sohani. M. D. . Homoepathy. , P.G.D.P.C.. Experience in Homoeopathy. Practising from 1994 ( 18 years ). B.H.M.S. & M.D.- . Study of . solanaceae. plant family to treat . behavioural. Our Inspiration . Our Mentors . In a path-breaking initiative,. PRANA - The world’s first Homoeopathy Yoga Centre brings together two specialized and complementary sciences that ensure holism in our understanding and journey towards true health. . Thalassemia. Prof. Firoza Begum. High Risk Pregnancy & Infertility Specialist. Chairman, Fetomaternal Medicine . Dept. , BSMMU. Introduction. Hemoglobinopathies. are among the most common inherited diseases.. BY A COMPUTATIONAL METHOD. Yulia Einav. Holon Institute of Technology. Israel. Outline. Introduction. Sys. tem. desi. g. n. Results. Summary & Conclusions. Acknowledgements. α and β thalassemia are the most common . Ministry of AYUSH. By. :. Dr. . K.S.Sethi. Advisor (Homoeopathy). Ministry of AYUSH. Government of INDIA. E-mail: . ks.sethi57@nic.in. Independent Ministry for AYUSH systems was constituted by Government of India on 9. MD; FRCP (London); . FRCPEdin. ; . FRCSEdin. T. halassemia. Hemoglobin molecule. : is the iron-containing oxygen-transport . metalloprotein. in the red blood cells of all vertebrates.. The normal . haemoglobin. Thalassemia . is an inherited blood disorder in which the body makes an abnormal form of hemoglobin. Hemoglobin is the protein molecule in red blood cells that carries oxygen. Hemoglobin is formed by the combination of . : are genetic(AR) disorders in . globin. chain production. . In individuals with β. -thalassemia. , there is either: . complete. absence of β-globin gene production . (β. 0. -thalassemia). (In 19. th. and 20. th. . Centurry. ). History – 19. th. Century. Homoeopathy was born in Germany .At the same time it came into England.. In 1826 Dr. Frederick Foster Harvey . Quin. (12.02.1799-28.11.1878), went to live in Germany and while travelling came across this new system of Medicine namely “Homoeopathy.”. Dr. Lincy . Ramteke. Professor in . Obs. & . Gyne. Gandhinagar. . Homoeo. Medical College. Gandhinagar. , Ahmedabad.. Learning Objectives. Systems of healing medicine. Meaning of homoeopathy. Origin of Homoeopathy. 1- what is the mode of inheritance in the vast majority f spherocytosis cases?. Autosomal dominant. Autosomal recessive. X-linked dominant. X linked recessive. 2- The amino acid present at the sixth position of the normal alpha-globin chain is replaced by which one of the following amino acids in sickle cell disease?. Newborn Screening ACT Sheet Beta Thalassemia Major(Hemoglobin F [Fetal] Only) Contact the family to inform them of the screening result.Evaluate infant, assess for splenomegaly, and do complete blood To the Editor,Coinheritance of hereditary spherocytosis ,HS) thalassemia is very rare. HS is a familial haemolytic disorder resulting from primary abnormality of red cell membrane. It is transmitted
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