PPT-Haemophilia in practice

Author : tatyana-admore | Published Date : 2017-03-23

Dr C E du Toit Groote Schuur Hospital An inherited Xlinked lifelong bleeding disorder affecting males almost exclusively Factor VIII deficiency Haemophilia A Factor

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Haemophilia in practice: Transcript


Dr C E du Toit Groote Schuur Hospital An inherited Xlinked lifelong bleeding disorder affecting males almost exclusively Factor VIII deficiency Haemophilia A Factor IX deficiency Haemophilia B. of the . Efficacy of. Prophylactic Use . of . rFIXFc and . rFIX. . Products and . Simulation . of the . Effect . of . Compliance on Effectiveness. Alfonso . Iorio. , MD, PhD. 13 May 2014. A. lfonso Iorio,. Sex linkage . and multiple alleles. Starter – sickle cell anaemia. Genotype. Hb. A. Hb. A. Hb. A. Hb. S. Hb. S. Hb. S. Phenotype. Normal. Sickle cell trait. Sickle cell anemia. Type of heamogolbin. New Zealand Haemophilia Treatment Centres provide comprehensive and specialized care for people with haemophilia and bleeding disorders. North Island Auckland Auckland Haemophilia Centre Level 5 , P. roprioception. and the Aging . H. emophilia . P. opulation. Bruno UK Steiner, PT,MT. The Anatomical Works. 4/24/12. Great Plains Regional Hemophilia Providers Meeting. HIV. HCV. https://www2a.cdc.gov/ncbddd/htcweb/UDC_Report. Alfonso . Iorio. . MD, PhD. McMaster. University. Canada. BeneF. ix. ®. (. nonacog. . alfa. ) is . not currently approved . for once-weekly prophylaxis . treatment. Alfonso Iorio. Bayer, . Biogen. 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.. Ward 34 day area. Ninewells. Hospital. juneward@nhs.net. Warfarin. reduces rate of stroke. Warfarin. remains one of the most dangerous medicines causing harm. Tayside has one of the most sophisticated services offering near patient testing, primarily nurse- led services with some pharmacy practitioners. Edin. ). Haemostasis-blood must be maintained in a fluid state in order to function as a transport system, but must be able to solidify to form a clot following vascular injury in order to prevent excessive bleeding, a process known as haemostasis. It is localised to the tissue damage and is followed by removal of the clot and tissue damage.. Alfonso Iorio, MD, PhD. Health Information Research Unit & Hemophilia Program. McMaster. University. Canada. Alfonso Iorio. Baxter . (Bayer, . Biogen. Idec, . NovoNordisk. , Pfizer . - No conflicts). EPISODE SIX| THIS PATHOLOGICAL LIFE BLUE BLEEDING Inherited bleeding conditions Definition:groupofconditionsthat HISTORY AlexeisufferedfromHaemophiliaB/Christmasdisease.BloodlinefromQueenVictoria.Howe notprovideresourcesfortreatingrare,chronic,andexpensiveconditions(suchashaemophilia)sincetheyfocustheirlimitedresourcesonpublichealthissuesthataffectlargerportionsofthepopulation,e.g.familyplanning,sa perspectives . and . the Kenyan Situation. .. Dr. Festus . Njuguna. Moi. University/MTRH. INTRODUCTION. Genetic X-linked disorder. Haemophilia. A and B. Affects 1 per 10,000 deliveries. 30% of cases due to new mutations. Amy Crowther. What is Haemophilia?. Haemophilia is a coagulation disorder.. The responsibility of blood clotting is down clotting factors in the blood. People with haemophilia have low levels of Factor VIII and Factor IX.. Alfonso Iorio, MD, PhD. Health Information Research Unit & Hemophilia Program. McMaster. University. Canada. Alfonso Iorio. Biogen. . Idec . (Bayer, Baxter, . NovoNordisk. , Pfizer - No conflicts).

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