PPT-Immune thrombocytopenic purpura (ITP)
Author : riley | Published Date : 2022-06-15
Ali Al Khader MD Faculty of Medicine AlBalqa Applied University Email alialkhaderbauedujo ITP 2 clinical subtypes 1Chronicrelatively common women between 20 amp
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Immune thrombocytopenic purpura (ITP): Transcript
Ali Al Khader MD Faculty of Medicine AlBalqa Applied University Email alialkhaderbauedujo ITP 2 clinical subtypes 1Chronicrelatively common women between 20 amp 40. Abstract. Immune thrombocytopenic purpura (ITP), also known as idiopathic thrombocytopenic purpura is thought to be due to autoimmune disease. An abnormal autoantibody (immunoglobulin G) binds to the platelet membrane, causing removal by the spleen. If left untreated it could lead to bleeding and possibly death (. DEAD OR ALIVE?. $10,000,000 REWARD. Adam R. Solomon. ITP, University of Heidelberg. April 15. th. , 2015. Why bimetric gravity?. Old CC problem: why isn’t . Λ. huge?. New CC problem: why is . Λ . Ophthalmic manifestation of congenital protein C deficiency Dr Shahla ansary peiatric heamatologyonclogist Dr Amir hesabi Assistant pediatric hematologyoncologist Case 1 CC: purpura fulminans Curtis Barry, MD. UMASS ECHO. April 28, 2017. Disclosure. I have no financial disclosures related to this subject. Background. HCV primarily affects the liver but other organ systems can become involved. Adapted from Rodeghiero F et al Blood 2009113238693 12 months Chronic ITP Persistent ITP Novartis Singapore . P3 approval #. SG2010199741 Exp. 18-Oct-2022. Disclaimer. “This presentation/slide deck may include data on an indication that has not been approved or cleared for use in Singapore by the Health Sciences Authority. It is intended to provide you with pertinent scientific data to form your own conclusions and make your own decisions. Information in this presentation/slide deck is not intended to be promoting or recommending any indication, dosage or other claim not covered in the licensed product information. Novartis does not support the promotion of its products in a manner inconsistent with its approved labelling.”. (IT) . are characterized . by . platelet size abnormalities . and it has been suggested . that this . parameter is useful for their differentiation from immune . thrombocytopenia. (. ITP. ). Recently, a . Winter 2018. agenda. Background information. See . BrICC. Documentation Checklist and “What Works What Doesn’t” on . InfoCDS. You may refer to prior ITPs for background info on your client; however, make sure to . Name/number of IT Policy. Domain Owner. Date. Educational Webinar Objectives. Provide an overview on the newly published . ITP Title and number. Policy background. Needs and drivers. Primary policy objectives. Associations. @. ConstructionSum. @. Constructionsummits. Construction Summits. Mike Buss. Head of Quality, Taylor Woodrow. ConSIG. Competency Working Group Chair. Construction Special Interest Group (. Gayla Oakley RN, CCRP, MAACVPR. Dir. Cardiology Services and Prevention. Boone County Health Center. Albion, Nebraska. Why How. o. This Photo. by Unknown Author is licensed under . a a a T I P Idiopathic Thrombocytopenic Purpura 32 Childhood Immune Thrombocytopenia: Long-term Follow-up Data Evaluated by the Criteria of the International Working Group on Immune Immune thrombocytopenia (ITP) is a common bleeding disorder in c clastic. vasculitis. . The . majority of cases occur as sequelae to strangles. However, Cases also occur following. . immunization against . S. . equi. . and as sequelae to infection with other streptococci..
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