Early deaths in Jamaican children with sickle cell disease.

In Jamaican children with homozygous sickle cell (SS) disease diagnosed at birth two-year survival was 87%, compared with 95% in children with sickle cell-haemoglobin C (CS) disease, and 99% in normal controls. Death among those with SS disease occurred most often between the ages of 6 and 12 months...

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Библиографические подробности
Главные авторы: Rogers, D W, Clarke, J M, Cupidore, L, Ramlal, A M, Sparke, B R, Serjeant, G R
Формат: Artigo
Язык:Inglês
Опубликовано: 1978
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Research Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC1605039/
https://ncbi.nlm.nih.gov/pubmed/656779
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