Congenital Bilateral Horizontal Gaze Palsy in a Brother and Sister

1980 ◽  
Vol 17 (4) ◽  
pp. 224-226
Author(s):  
Martin Ehrenberg ◽  
Walter M Jay ◽  
Linas A Sidrys ◽  
Karl J Fritz
Keyword(s):  
2014 ◽  
Vol 45 (S 01) ◽  
Author(s):  
J. Koch ◽  
F. Landauer ◽  
T. Keindl ◽  
M. Sloman

2005 ◽  
Vol 72 (1) ◽  
pp. 86-86 ◽  
Author(s):  
Vimla Menon ◽  
Rohit Saxena ◽  
Zia Chaudhary

1999 ◽  
Vol 36 (1) ◽  
pp. 47-49
Author(s):  
Panagiota Stavrou ◽  
Harry E Willshaw
Keyword(s):  

1980 ◽  
Vol 17 (4) ◽  
pp. 324-324 ◽  
Author(s):  
E K Dretakis
Keyword(s):  

2011 ◽  
Vol 59 (2) ◽  
pp. 162 ◽  
Author(s):  
NitinR Jain ◽  
Jitendra Jethani ◽  
Kalpana Narendran ◽  
L Kanth

2016 ◽  
Vol 10 (1) ◽  
pp. 126-128 ◽  
Author(s):  
Jesper Skovlund Jørgensen ◽  
Lisbeth Landschoff Lassen ◽  
Marianne Wegener

We report a case of lithium-induced downbeat nystagmus and horizontal gaze palsy in a 62-year-old woman who was treated for a bipolar affective disorder with lithium carbonate for one month. At presentation serum lithium was within therapeutic range. No alternative causes of the ocular motility disturbances were found, and the patient improved significantly as lithium carbonate was discontinued.


Author(s):  
John G. Morris ◽  
Padraic J. Grattan-Smith
Keyword(s):  

BMC Neurology ◽  
2019 ◽  
Vol 19 (1) ◽  
Author(s):  
Amirhossein Akhavan Sigari ◽  
Masoud Etemadifar ◽  
Mehri Salari

Abstract Background Demyelinating central nervous system diseases include several disorders that multiple sclerosis (MS) is identified as the most common among them. Ocular movement disturbances are a typical presentation in MS patients where lesions affect the complex and interconnected pathways involved in eye motion. Centers for gaze control are located in the pons primarily; therefore, lesions involving these centers can be presented with abnormalities in gaze. However, bilateral lesions in pontine gaze centers are exceptionally rare. Case presentation A 16-year-old girl with bilateral horizontal gaze palsy was referred to the neurology clinic. Magnetic resonance imaging of the patient indicated bilateral hyperintensities in the pons at the level of the paramedian pontine reticular formation. The patient was diagnosed with multiple sclerosis with respect to clinical and imaging findings and managed. Conclusion Ocular movement abnormalities are a commonly encountered manifestation in patients with multiple sclerosis, however, bilateral gaze palsy is an exceptionally rare sign and should guide the physician to contemplate for anticipated lesions in the pons, and suspect MS, especially in childbearing-aged women. Although an extensive workup should also be done to rule out possible mimickers.


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