Version 1
: Received: 10 June 2020 / Approved: 15 June 2020 / Online: 15 June 2020 (13:22:06 CEST)
How to cite:
Klocke, P.; Whalen-Browne, A.; Hepworth, E.; Panju, M. Occurrence of Balínt Syndrome in a Patient with Hypereosinophilic Syndrome. Preprints2020, 2020060195. https://doi.org/10.20944/preprints202006.0195.v1.
Klocke, P.; Whalen-Browne, A.; Hepworth, E.; Panju, M. Occurrence of Balínt Syndrome in a Patient with Hypereosinophilic Syndrome. Preprints 2020, 2020060195. https://doi.org/10.20944/preprints202006.0195.v1.
Cite as:
Klocke, P.; Whalen-Browne, A.; Hepworth, E.; Panju, M. Occurrence of Balínt Syndrome in a Patient with Hypereosinophilic Syndrome. Preprints2020, 2020060195. https://doi.org/10.20944/preprints202006.0195.v1.
Klocke, P.; Whalen-Browne, A.; Hepworth, E.; Panju, M. Occurrence of Balínt Syndrome in a Patient with Hypereosinophilic Syndrome. Preprints 2020, 2020060195. https://doi.org/10.20944/preprints202006.0195.v1.
Abstract
Balínt Syndrome is an acquired disorder manifesting in the inability to recognize several objects at once (simultagnosia), inaccurate visually guided limb movements despite intact motor function (optic ataxia) and the inability to make accurate voluntary saccades to visual targets despite demonstrating unrestricted range of eye movements (ocular motor apraxia). Here we report the first case of a patient presenting with Balínt Syndrome caused by a platelet-derived growth factor receptor A mutation (PDGFRA)-induced Hypereosinophilic Syndrome (HES).
Copyright:
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.