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Makulopathie bei Sichelzellerkrankung.
Maculopathy in sickle cell disease

URN to cite this document:
urn:nbn:de:bvb:355-epub-447166
DOI to cite this document:
10.5283/epub.44716
Bachmeier, Isabel ; Blecha, Christiane ; Föll, Jürgen ; Wolff, Daniel ; Jägle, Herbert
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License: Creative Commons Attribution 4.0
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Date of publication of this fulltext: 02 Feb 2021 15:05

This publication is part of the DEAL contract with Springer.


Abstract

Background Sickle cell disease (SCD) is a hereditary hemoglobinopathy, which leads to microcirculatory disturbances of various organ systems through recurrent vaso-occlusive episodes, with a possibly fatal outcome. Sickle cell retinopathy (SCR) is the best described ocular manifestation of SCD. Irrespective of the presence of peripheral SCR, sickle cell maculopathy (SCM) can occur early in the ...

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