| Literature DB >> 6196049 |
J F Talbot, A C Bird, G R Serjeant.
Abstract
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.Entities:
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Year: 1983 PMID: 6196049 PMCID: PMC1040197 DOI: 10.1136/bjo.67.11.777
Source DB: PubMed Journal: Br J Ophthalmol ISSN: 0007-1161 Impact factor: 4.638