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dc.contributor.authorMigowa, AN
dc.contributor.authorMurungi, CW
dc.contributor.authorGatinu, BW
dc.contributor.authorMbithe, J
dc.contributor.authorKimani, E
dc.contributor.authorOkiro, P
dc.contributor.authorRana, FS
dc.contributor.authorOchieng, R
dc.contributor.authorNduati, RW
dc.date.accessioned2013-06-12T10:07:39Z
dc.date.available2013-06-12T10:07:39Z
dc.date.issued2010-09
dc.identifier.citationEast Afr Med J. 2010 Sep;87(9):389-92en
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/23457818
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/32170
dc.description.abstractSevere congenital skin abnormalities are a rare event. This case is unique in that it is a case of harlequin ichthyosis in sub-sahara Africa in a child of African origin and elaborates the challenges faced in its management. We present a neonate who was managed for this condition at Chogoria Mission Hospital. In presenting this case, we aim to sensitise healthcare providers to promptly recognise and manage this rare skin condition.en
dc.language.isoenen
dc.publisherUniversity of Nairobien
dc.titleHarlequin ichthyosis in an African child: case report.en
dc.typeArticleen
local.publisherSchool of medicine,University of Nairobien


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