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Retinal changes in sickle cell/hereditary persistence of fetal haemoglobin syndrome.
  1. J F Talbot,
  2. A C Bird and
  3. 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.

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