منابع مشابه
Cold, season, and incidence of bells palsy
Bell’s palsy is a relatively common disease characterized by the sudden onset of unilateral facial paralysis. Using a centralized system that contains demographic data, the authors estimated rates, trends, and demographic risk of Bell’s palsy during a 2-year period. There were 140 incident cases of Bell’s palsy among patients referring to private clinics (a total of 6500 patients). The crude in...
متن کاملCold, season, and incidence of bells palsy
Bell’s palsy is a relatively common disease characterized by the sudden onset of unilateral facial paralysis. Using a centralized system that contains demographic data, the authors estimated rates, trends, and demographic risk of Bell’s palsy during a 2-year period. There were 140 incident cases of Bell’s palsy among patients referring to private clinics (a total of 6500 patients). The crude in...
متن کاملSixth nerve palsy + ipsilateral Horner's Syndrome = Parkinson's Syndrome.
PURPOSE To present five patients with VIth nerve palsy and ipsilateral Horner's Syndrome (HS), as a result of cavernous sinus alteration. STUDY DESIGN Consecutive case series. MATERIAL AND METHODS Five patients presented abducens palsy with horizontal diplopia (3 in primary position and 2 in lateral gaze only) and ipsilateral HS. Apraclonidine 0.5% drops evidenced sympathetic denervation in...
متن کاملMidbrain infarction causing oculomotor nerve palsy and ipsilateral cerebellar ataxia.
We herein report the case of an 81-year-old woman with midbrain infarction causing pupil-sparing oculomotor nerve palsy with ipsilateral cerebellar ataxia. The lesion was located at the rostral end of the decussation of the superior cerebellar peduncle touching the dorsal side, further caudal and dorsal to causal lesions of Claude's syndrome, which presented as oculomotor palsy and contralatera...
متن کاملIpsilateral stroke in a patient with horizontal gaze palsy with progressive scoliosis and a subcortical infarct.
BACKGROUND AND PURPOSE horizontal gaze palsy with progressive scoliosis (HGPPS) is a rare congenital disorder caused by mutation in the ROBO3 gene. It is characterized by absent horizontal eye movements with progressive scoliosis developing in childhood and adolescence. To our knowledge, both diffusion tensor imaging evaluation in HGPPS patients who present with stroke and truncating stop codon...
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ژورنال
عنوان ژورنال: Journal of Neurology, Neurosurgery & Psychiatry
سال: 2005
ISSN: 0022-3050
DOI: 10.1136/jnnp.2004.043059