Retinal changes in sickle cell/hereditary persistence of fetal haemoglobin syndrome.
AUTOR(ES)
Talbot, J F
RESUMO
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.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1040197Documentos Relacionados
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