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Isolated Oculomotor Nerve Palsy in Mild Traumatic Brain Injury

American Journal of Physical Medicine & Rehabilitation, 2020
Supplemental digital content is available in the text. Background Isolated oculomotor nerve palsy is rarely encountered after mild traumatic brain injury.
Taeyeon Kim, Kiyeun Nam, B. Kwon
semanticscholar   +1 more source

OCULOMOTOR NERVE PALSY IN CHILDHOOD

Australian and New Zealand Journal of Ophthalmology, 1987
Abstract Oculomotor nerve palsy was found in 28 children. Trauma was the cause in seven, infection in six. while tumour, poison and migraine were each responsible for one case. Twelve cases were cryptogenic: eight of these were present at birth (but three were probably due to birth trauma), and four cases appeared in infancy, but with no cause found ...
openaire   +2 more sources

Surgical Management of Oculomotor Nerve Palsy

American Journal of Ophthalmology, 1991
We treated seven patients with unilateral oculomotor nerve palsy by transposition of the insertion of the superior oblique tendon to a point anterior and medial to the insertion of the superior rectus muscle without trochleotomy (Scott procedure). Additionally, large recessions of the lateral rectus muscle of involved eyes and, occasionally, recess ...
I, Gottlob, R A, Catalano, R D, Reinecke
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Isolated oculomotor nerve palsy in lymphoma

Neurological Research, 2000
We report a patient with non-Hodgkin's lymphoma who developed a unilateral left oculomotor nerve palsy. Only eyelid lifting and vertical gaze were involved. Lateral gaze or sizes and light reactions of pupils were not involved. Magnetic resonance imaging revealed an enhancement of an upper part of left cavernous sinus and the posterior clinoid process.
Y, Manabe   +3 more
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Managing the patient with oculomotor nerve palsy

Current Opinion in Ophthalmology, 2013
To provide clinically relevant information regarding the evaluation and current treatment options for oculomotor nerve palsies. We survey recent literature and provide some insights into these studies.Recent case reports highlight emerging new causes of oculomotor cranial nerve palsies, including sellar chordoma, odontogenic abscess, nonaneurysmal ...
Karthikeyan A, Sadagopan   +1 more
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Pathology of oculomotor nerve palsy in diabetics

Neurology, 1970
SUMMARYThe pathological findings of pupil-sparing oculomotor palsy in a diabetic patient are presented and discussed in view of the 2 other published necropsy studies of this disorder. Intraneural arteriolar abnormalities were seen in all 3, but our patient was the first in whom the pathological neural process involved the subarachnoid segment of the ...
R B, Weber, R B, Daroff, E A, Mackey
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Inferior branch palsy of the oculomotor nerve

Annals of Neurology, 1977
AbstractThree patients with inferior branch palsies of the oculomotor nerve are described. Two were under 10 years of age and the third was 30 years old at the onset. All 3 presented with painless diplopia. The onset was sudden in 2 patients and progressive in the third.
J O, Susac, W F, Hoyt
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Fascia lata augmented nasal transposition of split lateral rectus in complete oculomotor nerve palsy with a previous failed surgery

European Journal of Ophthalmology, 2020
Purpose: To report our experience in the management of a complete oculomotor nerve palsy with a previous failed surgery. Methods: We used a fascia lata augmented nasal transposition of the split lateral rectus in a patient who had complete oculomotor ...
Chong-bin Tsai, Chien-Liang Fang
semanticscholar   +1 more source

Cryptogenic Oculomotor Nerve Palsies in Children

American Journal of Ophthalmology, 1985
We examined two cases of isolated, acquired, unremitting oculomotor palsies in children. The results of systemic, neurologic, and neuroradiologic investigations were normal. Both children were observed for more than two years and showed no additional signs or symptoms.
T R, Mizen, R M, Burde, T G, Klingele
openaire   +2 more sources

CHARGE syndrome with oculomotor nerve palsy

Journal of American Association for Pediatric Ophthalmology and Strabismus, 2015
CHARGE syndrome is a congenital disorder characterized by coloboma, heart defects, atresia of the choanae, retarded growth, genital hypoplasia, ear anomalies, and/or hearing loss. We report the case of a 2-year-old boy with CHARGE syndrome who presented with left exotropia and elevation deficit since infancy.
Hee Kyung, Yang   +5 more
openaire   +2 more sources

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