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    Harlequin ichthyosis in an African child: case report.

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    Date
    2010-09
    Author
    Migowa, AN
    Murungi, CW
    Gatinu, BW
    Mbithe, J
    Kimani, E
    Okiro, P
    Rana, FS
    Ochieng, R
    Nduati, RW
    Type
    Article
    Language
    en
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    Abstract
    Severe 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.
    URI
    http://www.ncbi.nlm.nih.gov/pubmed/23457818
    http://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/32170
    Citation
    East Afr Med J. 2010 Sep;87(9):389-92
    Publisher
    University of Nairobi
     
    School of medicine,University of Nairobi
     
    Collections
    • Faculty of Health Sciences (FHS) [10418]

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