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dc.contributor.authorAluoch, JR
dc.date.accessioned2013-06-06T14:37:41Z
dc.date.available2013-06-06T14:37:41Z
dc.date.issued1984
dc.identifier.citationTrop Geogr Med. 1984 Jun;36(2):115-22en
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/6332394
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/29474
dc.description.abstractThrough a questionnaire data were collected from 116 patients with sickle cell disease (SCD) in the Netherlands, about two thirds of all the patients with SCD in the country. Sixty-four percent of the patients are of Surinamese origin, 14% come from the Netherlands Antilles, 11% come from Turkey, and 11% from elsewhere. Two thirds of the patients live in Amsterdam and Rotterdam. Sixty-seven were children and 49 were adults. Sickle cell anaemia (SS disease) was found in 74, sickle cell beta thalassaemia (S beta thal) in 18, and sickle cell haemoglobin C(SC)-disease in 24 patients. Clinical features and treatment are discussed and the data are compared with the results of similar studies in other European countries.en
dc.language.isoenen
dc.titleSurvey of sickle cell disease in the Netherlandsen
dc.typeArticleen
local.publisherDepartment of Medicine, Faculty of Medicine, University of Nairobien


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