exotropia/glavobolja

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Treatment of Intermittent Exotropia of the Convergence Insufficiency Type with Bupivacaine 0.75%: 5-Year Experience and Outcomes.

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Bupivicaine has been shown to stimulate ocular muscle structure and length after injection into ocular muscles. Bupivicaine 0.75% has been utilized in the treatment of strabismus to alter ocular alignment by strengthening an ocular muscle. This study is designed to report 5-year

Vision therapy for basic exotropia in adults: 2 case studies.

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BACKGROUND Basic exotropia accounts for approximately 50% of all intermittent exotropias. Many clinicians view treating these patients, especially adults with childhood-onset exotropia, as challenging. Conflicting opinions still exist regarding prescribing any treatment for adult strabismics,

A Randomized Trial Evaluating Short-term Effectiveness of Overminus Lenses in Children 3 to 6 Years of Age with Intermittent Exotropia.

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To evaluate the short-term effectiveness of overminus spectacles in improving control of childhood intermittent exotropia (IXT). Randomized, clinical trial. A total of 58 children aged 3 to <7 years with IXT. Eligibility criteria included a distance control score of 2 or worse (mean of 3 measures

Objective improvement from base-in prisms for reading discomfort associated with mini-convergence insufficiency type exophoria in school children.

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OBJECTIVE To determine whether base-in prism glasses could diminish asthenopia, and improve reading abilities (speed, accuracy and comprehension). METHODS All patients aged 8-18 years, from one practice, were examined and considered prospectively over a six month period. Ten percent (72) of these

Accommodative spasm with bilateral vision loss due to untreated intermittent exotropia in an adult.

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BACKGROUND Intermittent exotropia (IXT) is an exodeviation intermittently controlled by fusional mechanisms. Patients with IXT may present with asthenopic symptoms, blurred vision, headaches, diplopia or visual confusion and reading difficulties; especially after prolonged periods of near

Devastating complications from alcohol cauterization of recurrent Rathke cleft cyst. Case report.

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Rathke cleft cysts are commonly found on autopsy but are seldom symptomatic. Conventional treatment of these lesions consists of transsphenoidal drainage with partial excision of the cyst, and recurrence is rare. Alternatively, the instillation of absolute alcohol into the cyst has been described in

[A case of post-infectious wall-eyed bilateral internuclear ophthalmoplegia (WEBINO) syndrome].

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The patient is a 72-year-old man who had tonsillitis and underwent incision on March 6, 1998. He complained headache and nausea from March 10 and double vision from March 12. He was admitted to our hospital on March 14. Neurological examination on March 18 revealed bilateral internuclear

High flow bypass for right giant cavernous internal carotid artery aneurysm with fibromuscular dysplasia of cervical internal carotid artery: microsurgical 2-D video

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Background: It is well known that intracranial aneurysms can be associated to fibromuscular dysplasia (FMD). Nevertheless, it is not clear the best treatment strategy when there is an association of giant symptomatic cavernous carotid

Frequency of undetected binocular vision anomalies among ophthalmology trainees

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Purpose: The use of ophthalmic instruments requires increased effort on the accommodation and vergence system. This study aimed to understand the prevalence of binocular vision anomalies among ophthalmology trainees attending a surgical

Endoscopic and trans-fornix removal of a giant orbital-ethmoidal osteoma.

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A 39-year old female was referred with a 2 year history of slowly progressive headache, exophthalmos, diplopia and restricted eye movements with exotropia of the right eye. Orthoptic examination revealed restricted elevation and mildly restricted adduction of the right eye. CT and MRI demonstrated a

[Presentation of two cases of Crouzon syndrome: allelic cranio-stenotic conditions of FGFR genes].

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BACKGROUND Craniosynostosis is an abnormal and premature fusion of any cranial suture. Twenty per cent of them involve any specific syndrome with Mendelian transmission; the other 80% are "non syndromic", although but 10-14% of them are genetically transmitted. Using the experience of two patients

[Surgical correction of esophorias].

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A report covering 80 cases of esophoria in which surgery was performed. All the patients had previously suffered from severe headache and other complaints. Preoperative treatment consisted of full prismatic correction. The power of the prisms was measured by the "Polatest" method. We observed that

Bilateral Internuclear Ophthalmoplegia in a Patient with Devic's Neuromyelitis Optica.

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An unusual presentation of Devic's neuromyelitis optica (NMO) disease associated with bilateral internuclear ophthalmoplegia (INO) is described. A 32-year-old pregnant patient was diagnosed with NMO. First symptoms were headache and sudden visual loss in her right eye (RE). Eighteen months ago, she

The need for optometric investigation in suspected Meares-Irlen syndrome or visual stress.

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Meares-Irlen syndrome is characterised by symptoms of eye strain, headaches and visual perceptual distortions when viewing text. The symptoms are alleviated with individually prescribed coloured filters, such as precision tinted lenses. Meares-Irlen syndrome, and the related condition of visual

Optometric function in visually sensitive migraine before and after treatment with tinted spectacles.

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Optometrists frequently encounter patients with migraine and patients and practitioners sometimes suspect that visual stimuli or visual anomalies trigger headaches. There is a lack of evidence-based research on the issue, however. Some patients with migraine may be hypersensitive to visual stimuli,

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