We can do more to identify patients with primary immunodeficiences

dc.contributor.authorVan den Berg, Sylvia
dc.contributor.authorVan Rooyen, Cathy
dc.contributor.authorGreen, Robin J.
dc.date.accessioned2017-09-15T04:54:10Z
dc.date.available2017-09-15T04:54:10Z
dc.date.issued2017-03
dc.description.abstractPrimary immunodeficiencies (PIDs) remain largely undiagnosed and underreported in South Africa.1 PIDs are inherited, non-communicable disorders that involve a defect in one or more components of the immune system. Immunodeficiencies comprise more than 250 heterogenous disorders that cause either an absent, defective or weakened function of the immune system.2 These disorders are mostly associated with recurrent infections that can present very early in childhood, but depending on the defect, also in later childhood and even in adulthood.en_ZA
dc.description.departmentPaediatrics and Child Healthen_ZA
dc.description.librarianam2017en_ZA
dc.description.urihttp://www.journals.co.za/content/journal/cacien_ZA
dc.identifier.citationVan den Berg, S., Van Rooyen, C. & Green, R.J. 2017, 'We can do more to identify patients with primary immunodeficiences', Current Allergy & Clinical Immunology, vol. 30, no. 1, pp. 44-52.en_ZA
dc.identifier.issn1609-3607
dc.identifier.urihttp://hdl.handle.net/2263/62263
dc.language.isoenen_ZA
dc.publisherAllergy Society of South Africaen_ZA
dc.rightsAllergy Society of South Africaen_ZA
dc.subjectPrimary immunodeficienciesen_ZA
dc.subjectPatientsen_ZA
dc.subjectImmune systemen_ZA
dc.subjectSouth Africa (SA)en_ZA
dc.subjectPrimary immunodeficiencies (PIDs)en_ZA
dc.titleWe can do more to identify patients with primary immunodeficiencesen_ZA
dc.typeArticleen_ZA

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