We can do more to identify patients with primary immunodeficiences

Show simple item record

dc.contributor.author Van den Berg, Sylvia
dc.contributor.author Van Rooyen, Cathy
dc.contributor.author Green, Robin J.
dc.date.accessioned 2017-09-15T04:54:10Z
dc.date.available 2017-09-15T04:54:10Z
dc.date.issued 2017-03
dc.description.abstract Primary 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.department Paediatrics and Child Health en_ZA
dc.description.librarian am2017 en_ZA
dc.description.uri http://www.journals.co.za/content/journal/caci en_ZA
dc.identifier.citation Van 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.issn 1609-3607
dc.identifier.uri http://hdl.handle.net/2263/62263
dc.language.iso en en_ZA
dc.publisher Allergy Society of South Africa en_ZA
dc.rights Allergy Society of South Africa en_ZA
dc.subject Primary immunodeficiencies en_ZA
dc.subject Patients en_ZA
dc.subject Immune system en_ZA
dc.subject South Africa (SA) en_ZA
dc.subject Primary immunodeficiencies (PIDs) en_ZA
dc.title We can do more to identify patients with primary immunodeficiences en_ZA
dc.type Article en_ZA


Files in this item

This item appears in the following Collection(s)

Show simple item record