Retinal changes in sickle cell/hereditary persistence of fetal haemoglobin syndrome
- PMID: 6196049
- PMCID: PMC1040197
- DOI: 10.1136/bjo.67.11.777
Retinal changes in sickle cell/hereditary persistence of fetal haemoglobin syndrome
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.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical