Hereditary elliptocytosis associated with severe haemolytic anaemia and malaria.

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dc.date.accessioned 2013-06-19T12:39:53Z
dc.date.accessioned 2017-10-16T13:05:32Z
dc.date.available 2013-06-19T12:39:53Z
dc.date.available 2017-10-16T13:05:32Z
dc.date.issued 1971
dc.identifier.citation Nkrumah, F. K. (1971). Oculoauriculovertebral dysplasia (Goldenhar's syndrome). Ghana Medical Journal, 10(1), 60-62. en_US
dc.identifier.uri http://197.255.68.203/handle/123456789/3658
dc.description.abstract A case of Goldenhar's Syndrome or Oculoauriculovertebral dysplasia in a Ghanaian infant is described. Significant were the additional findings of congenital esophageal atresia and arthrogryposis which have so far not been reported in association with the syndrome. en_US
dc.language.iso en en_US
dc.publisher Ghana Medical Journal en_US
dc.title Hereditary elliptocytosis associated with severe haemolytic anaemia and malaria. en_US
dc.type Article en_US


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  • Epidemiology Department [262]
    The Epidemiology Department contributes to the mission of the institute through basic and applied epidemiological research on, but not limited to, malaria and other diseases of public health importance. It is also home to the Social Science Unit of the Institute, including the Health Support Centre for HIV/AIDS and other communicable and noncommunicable health problems.

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