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Australasian journal of optometry, The, 2007
Horner syndrome is an uncommon but important clinical entity, representing interruption of the sympathetic pathway to the eye and face. Horner syndrome is almost always diagnosed clinically, though pharmacological testing can be used to confirm the diagnosis.
Gavin Wright +2 more
exaly +4 more sources
Horner syndrome is an uncommon but important clinical entity, representing interruption of the sympathetic pathway to the eye and face. Horner syndrome is almost always diagnosed clinically, though pharmacological testing can be used to confirm the diagnosis.
Gavin Wright +2 more
exaly +4 more sources
Current Opinion in Ophthalmology, 2003
Horner syndrome refers to the constellation of signs resulting from the interruption of sympathetic innervation to the eye and ocular adnexae. Classically, the clinical findings include a triad of ipsilateral blepharoptosis, pupillary miosis, and facial anhidrosis.
Kelly A, Walton, Lawrence M, Buono
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Horner syndrome refers to the constellation of signs resulting from the interruption of sympathetic innervation to the eye and ocular adnexae. Classically, the clinical findings include a triad of ipsilateral blepharoptosis, pupillary miosis, and facial anhidrosis.
Kelly A, Walton, Lawrence M, Buono
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Archives of Neurology, 1968
THE use of eponyms to denote medical syndromes is common among physicians and especially among neurologists. A disadvantage of this practice is that the names themselves are not descriptive. Furthermore, confusion arises when more than one person is credited with a single achievement or when one man's name is attached to several discoveries.
R H, Wilkins, I A, Brody
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THE use of eponyms to denote medical syndromes is common among physicians and especially among neurologists. A disadvantage of this practice is that the names themselves are not descriptive. Furthermore, confusion arises when more than one person is credited with a single achievement or when one man's name is attached to several discoveries.
R H, Wilkins, I A, Brody
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Archives of Ophthalmology, 1980
Patients with congenital Horner's syndrome (who seemed, on the basis of their clinical history and the distribution fo anhidrosis, to have a preganglionic lesion) had partial mydriatic failure with hydroxyamphetamine hydrobromide and a supersensitivity to phenylephrine hydrochloride.
J M, Weinstein +2 more
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Patients with congenital Horner's syndrome (who seemed, on the basis of their clinical history and the distribution fo anhidrosis, to have a preganglionic lesion) had partial mydriatic failure with hydroxyamphetamine hydrobromide and a supersensitivity to phenylephrine hydrochloride.
J M, Weinstein +2 more
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Horner's syndrome—not to be sneezed at
The Lancet, 2010Although no robust evidence is available for the routine use of anticoagulants, imaging studies suggest that most complications are due to thromboembolic events rather than insuffi cient fl ow. A retrospective analysis of 298 patients, found a 2-6% risk of subsequent ischaemic stroke with antiplatelet or anticoagulant therapy, with no signifi cant diff
Farid, Bazari +2 more
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Archives of Neurology, 1974
Although Horner syndrome is not a rare condition, little is known of the fact that the syndrome may, in some cases, alternate from one side to the other, which we will call "alternating Horner syndrome." Three patients with this peculiar syndrome had lower cervical lesions due to syringomyelia, Shy-Drager syndrome, and radiation myelopathy ...
T, Furukawa, Y, Toyokura
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Although Horner syndrome is not a rare condition, little is known of the fact that the syndrome may, in some cases, alternate from one side to the other, which we will call "alternating Horner syndrome." Three patients with this peculiar syndrome had lower cervical lesions due to syringomyelia, Shy-Drager syndrome, and radiation myelopathy ...
T, Furukawa, Y, Toyokura
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The diagnosis of Horner's syndrome
Journal of the Neurological Sciences, 1986We studied the accuracy of the clinical diagnosis of Horner's syndrome in 62 patients. The final criterion was serial photography of the darkness reflex of the pupil. This technique confirmed oculosympathetic dysfunction in only 50%. The positive predictive value of the clinical diagnosis could be increased to more than 80% by measuring the degree of ...
H L, van der Wiel, J, van Gijn
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Horner's syndrome in childhood
Neurology, 1976During a 36-month period, seven cases of Horner's syndrome were encountered in a general pediatric hospital. The most common site of involvement was the ipsilateral sympathetic chain, although multiple sites were involved. Several causes of Horner's syndrome in childhood that have received little previous attention are reported-internal carotid artery ...
C, Sauer, M W, Levingohn
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Journal of Pediatric Ophthalmology & Strabismus, 1988
ABSTRACT Ten cases of Horner's syndrome with pharmacologic testing and computed tomography scans are described in patients up to age 8 years. The patients also were assessed for iris color and facial sweating. Classical preganglionic Horner's syndrome associated with brachial plexus birth injury was not identified in any case.
G, Woodruff, J R, Buncic, J D, Morin
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ABSTRACT Ten cases of Horner's syndrome with pharmacologic testing and computed tomography scans are described in patients up to age 8 years. The patients also were assessed for iris color and facial sweating. Classical preganglionic Horner's syndrome associated with brachial plexus birth injury was not identified in any case.
G, Woodruff, J R, Buncic, J D, Morin
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