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Retinal changes in sickle cell/hereditary persistence of fetal haemoglobin syndrome.

We describe for the first time retinal changes in sickle cell/hereditary persistence of fetal haemoglobin syndrome, which is a rare and benign disorder. The changes are qualitatively similar to retinal disease seen with sickle haemoglobin and sickle C haemoglobin, but are mild.

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書目詳細資料
Main Authors: Talbot, J F, Bird, A C, Serjeant, G R
格式: Artigo
語言:Inglês
出版: 1983
主題:
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC1040197/
https://ncbi.nlm.nih.gov/pubmed/6196049
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