Platelet-derived growth factor receptor inhibition to treat idiopathic hypereosinophilic syndrome

2004 ◽  
Vol 31 ◽  
pp. 12-17 ◽  
Author(s):  
Richard M Stone ◽  
D.Gary Gilliland ◽  
Amy D Klion
2003 ◽  
Vol 75 (3) ◽  
pp. 334-339 ◽  
Author(s):  
Roope K. Sihvola ◽  
Jussi M. Tikkanen ◽  
Rainer Krebs ◽  
Eva M. Aaltola ◽  
Elisabeth Buchdunger ◽  
...  

Author(s):  
Philipp Klocke ◽  
Anna Whalen-Browne ◽  
Elliot Hepworth ◽  
Mohamed Panju

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).


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