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East Afr Med J ; 87(9): 389-92, 2010 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-23457818

RESUMO

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.


Assuntos
Ictiose Lamelar/patologia , Ictiose Lamelar/terapia , África Subsaariana , Evolução Fatal , Humanos , Recém-Nascido , Masculino
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