Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/5187
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dc.contributor.authorOsafo-Kwaako, Alfred-
dc.contributor.authorKiman, Kahaki-
dc.contributor.authorlIako, Dunera-
dc.contributor.authorAkafo, Stephen-
dc.contributor.authorEkem, Ivy-
dc.contributor.authorOnike, Rodrigues-
dc.contributor.authorEnweronu-Laryea, Christabel-
dc.contributor.authorNentwich, Martin M.-
dc.date.accessioned2021-03-26T11:07:10Z-
dc.date.available2021-03-26T11:07:10Z-
dc.date.issued2010-10-
dc.identifier.urihttp://hdl.handle.net/123456789/5187-
dc.description.abstractSickle cell hemoglobinopathies are a group of inherited diseases characterized by an abnormality in the ~-chain of the hemoglobin molecule. Sickle cell disease (SCD) is found all over the world except in the Far East and in the Arctic countries. It is most common in Africans and people of African descent but also occurs in the non-black population of Saudi Arabia and India.en_US
dc.language.isoenen_US
dc.subjectOcular manifestationsen_US
dc.subjectsickle cell diseaseen_US
dc.subjectEpidemiologyen_US
dc.titleOcular manifestations of sickle cell disease at the Korle-bu Hospital, Accra, Ghanaen_US
dc.typeArticleen_US
Appears in Collections:School of Medical Sciences

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