PPT-Immunodeficiency (1 of 2)
Author : heavin | Published Date : 2022-02-16
Ali Al Khader MD Faculty of Medicine AlBalqa Applied University Email alialkhaderbauedujo Primary immunodeficiency diseases Innate or adaptive Most are detected
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Immunodeficiency (1 of 2): Transcript
Ali Al Khader MD Faculty of Medicine AlBalqa Applied University Email alialkhaderbauedujo Primary immunodeficiency diseases Innate or adaptive Most are detected in infancy 6 months 2 years . Martin Liška. Immunodeficiency. = a disorder of immune system which manifests by impaired ability to carry out basic immunological functions, primarily defence against infection or immunological surveillance. . One infection. too many!. Dr. Ahmad AlKhabaz. , MBBS, FRCPC. Head of Pediatric Allergy & Clinical Immunology . U. nit. Chair of the allergy & immunology exam committee (KIMS). Tutor for the pediatric residency program (KIMS). (HIV). Independent Nursing Studies . NURS 420. . Student Presentation. Objectives. :. History of illness . Definition. OTHER NAMES FOR HIV. Pathophysiology. Diagnosis. Etiology . Signs and symptoms. Iga. deficiency - description. Description:. Serum IgA <5 mg/. dL. Normal serum IgG and IgM. Patients >1 year . Genetics:. Autosomal Dominant. Abnormalities on Chromosome 18. Associated with HLA-A1, HLA-A2, B8, and Dw3 . Mutua C, . Karimi. . D, . Irungu. . A, . Patil. . R, . Ngwatu. . P, . Manguyu. W . Kiptum. D. Gertrude’s Children Hospital Nairobi, Kenya. Outline . Background. Methods. Case presentation. Anna Postolova, MD MPH. Allergy/Immunology/Rheumatology. Menlo Medical Clinic. Stanford Health Care . Disclosures . Nothing to disclose. Objectives. Recognize aspects of history and presentation that are suggestive of a primary immunodeficiency or immune dysregulatory syndrome in rheumatology patients. David Lowe. Royal Free Hospital / University College London. Or…. Suspecting primary immunodeficiency. AND. Suspecting secondary . hypogammaglobulinemia. Primary immunodeficiency (…in adults). Antibodies / B cells. For MBBS (29.09.2017). By: . Dr. . . Puneet Kumar Gupta. Assistant Professor, M. icrobiology. ,. Introduction. . Immunodeficiency . diseases. Defence . mechanisms of . body are impaired→ repeated . Severe Combined Immunodeficiency (SCID). What is SCID?. Severe . Combined . Immunodeficiency, otherwise known as SCID.. SCID is a group of very rare-and potentially fatal-inherited disorders related to the immune system. . Dr. . Mayssaa. . Essam. Immunodeficiency . . . The . immunodeficiency may be the result of defective immunity, both innate and specific, because of . genetic. abnormality (. primary. ) or there is a loss of function because of the damage by . Immunodeficiency Diseases. Innate Immune System. Adaptive Immune System. Innate Immune system:. Physical epithelial barriers. Phagocytic leukocytes (Monocytes/Macrophages, . Neutophils. ). Dendritic cells.. Patients with primary immunodeficiency diseasesmost often are recognized because of their increased(Table 2). In fact, non-infectious manifestations, suchodeficiency. Other immunodeficiency diseases m Hypersensitivities. Hypersensitivity. Any immune response against a foreign antigen exaggerated beyond the norm. Four types. Type I (immediate). Type II (cytotoxic). Type III (immune complex–mediated). Immunodeficiency. = a disorder of immune system which manifests by impaired ability to carry out basic immunological functions, primarily defence against infection or immunological surveillance. Immunodeficies.
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