Pseudobulbar Palsy

2020 ◽  
pp. 152-154
Author(s):  
K. Gupta ◽  
P. Carmichael ◽  
A. Zumla
Keyword(s):  
2003 ◽  
Vol 1 (5) ◽  
pp. 27-30
Author(s):  
Liu Xiang-hua ◽  
Tang Li-xin ◽  
Liu Ai-zhen ◽  
Zhang Xue-li ◽  
Du Lin ◽  
...  

2004 ◽  
Vol 15 (2) ◽  
pp. 128-130
Author(s):  
Adrià Arboix ◽  
Imgard Costa ◽  
Carles Besses ◽  
Jordi Sans-Sabrafen

1989 ◽  
Vol 25 (6) ◽  
pp. 547-554 ◽  
Author(s):  
Ruben Kuzniecky ◽  
Frederick Andermann ◽  
Donatella Tampieri ◽  
Denis Melanson ◽  
Andre Olivier ◽  
...  

1989 ◽  
Vol 3 (7) ◽  
pp. 50
Author(s):  
J Gordon Millichap
Keyword(s):  

Author(s):  
D. Bogdanova ◽  
I. Milanov ◽  
D. Georgiev

ABSTRACT:Background:The central nervous system is often involved in Behcet's disease. Most common are meningoencephalitic and brain stem syndromes. Although basal ganglia involvement is not an uncommon finding on necropsy, there are only single reports on extrapyramidal syndromes-dyskinesia, chorea and Parkinsonism in patients with Behcet's disease.Case study:We report a patient fulfilling the criteria of the International Study Group for Behcet's disease. He had recurrent oral ulcerations, bilateral posterior uveitis and retinal vasculitis, skin papules and pustules, and recurrent monoarthritis. Neurologic examination revealed pseudobulbar palsy, slight and asymmetric bilateral pyramidal syndrome, muscle rigidity involving the four limbs, bradykinesia, masked face, and impaired postural reflexes. There was postural tremor in the extremities and myoclonic jerks involving the tongue and face muscles. Magnetic resonance imaging demonstrated small bilateral multifocal hyperintense lesions, with right predilection, involving the periventricular white matter, brain stem and basal ganglia.Conclusions:The Parkinsonian syndrome found in our patient might be due to involvement of both substantia nigra and basal ganglia. This case further emphasizes the wide spectrum of the neurological manifestations of Behcet's disease


2019 ◽  
Vol 12 (12) ◽  
pp. e232061
Author(s):  
Masanori Nagaoka ◽  
Hiromasa Suzuki ◽  
Kazuhiro Kanayama ◽  
Yuko Ozone

2019 ◽  
Vol 11 (3) ◽  
pp. 319-324 ◽  
Author(s):  
Fumihito Yoshii ◽  
Hiromi Sugiyama ◽  
Kazuyuki Kodama ◽  
Takahito Irino

Foix-Chavany-Marie syndrome (FCMS) is a rare type of pseudobulbar palsy characterized by automatic-voluntary dissociation of movements of the face, tongue, pharynx, and masticatory muscles. Most cases are due to bilateral ischemic lesions of the anterior operculum, but the syndrome has also been described after unilateral opercular damage, either isolated or associated with contralateral cortico-nuclear tract involvement. We report a patient with FCMS due to right anterior opercular lesion with contralateral infarction of the corona radiata. The patient presented with paralysis of the face and tongue with automatic and voluntary dissociation. To our knowledge, FCMS with this peculiar lesion topography has rarely been reported. We discuss the underlying mechanism with reference to MRI and diffusion tensor imaging.


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