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dc.contributor.authorMacharia, W M
dc.contributor.authorMbaabu, C
dc.contributor.authorWachira, L
dc.contributor.authorMuhudhia, S O
dc.contributor.authorMoniz, G
dc.date.accessioned2013-06-07T11:44:46Z
dc.date.available2013-06-07T11:44:46Z
dc.date.issued2005-11
dc.identifier.citationEast Afr Med J. 2005 Nov;82(11):598-600.en
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/16463755
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/30017
dc.description.abstractAngio-oedema may be hereditary or acquired and is characterised by episodes of potentially life threatening localised tissue oedema and swelling resulting from deficiency of compliment pathway C1 esterase inhibitor. Acquired angio-oedema is about ten times less frequent than the hereditary type and has been associated with immune-deficiency disorders, malignancies and exposure to specific medications and food substances. We present a case of seven year old, human immune-deficiency virus positive girl, who developed gross swelling of the tongue and neck while on treatment for pneumococcal meningitis with ceftriaxone. Difficulties in arriving at a definitive diagnosis of angio-oedema in a resource poor country are discussed and alternative diagnostic options proposeden
dc.language.isoenen
dc.publisherUniversity of Nairobi.en
dc.titleCeftriaxone or HIV associated angio-oedema? Case reporten
dc.typeArticleen
local.publisherDepartment of Paediatrics and Child Health, College of Health Sciences, University of Nairobi, Kenyaen


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