diplopia/atrophy

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Management of ocular torsion and diplopia after macular translocation for age-related macular degeneration: prospective clinical study.

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OBJECTIVE To report the results of a prospective clinical series to evaluate the management of both torsion and diplopia in a large group of patients after full macular translocation (FMT) and extraocular muscle surgery. METHODS Prospective interventional case series. METHODS Information gathered

Diplopia and Ptosis as the Initial Manifestations of Acquired Hepatocerebral Degeneration.

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[Surgical treatment of diplopia in patients with Graves' ophthalmopathy].

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OBJECTIVE To investigate the timing and effect of surgical treatment of diplopia caused by hypertrophic inferior rectus in patients with Graves' ophthalmopathy and pathologic changes of inferior recti. METHODS Eleven diplopic patients with restrictive superior motion and enlarged inferior recti

Fresnel prism correction for trauma-induced diplopia.

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Fresnel prisms placed on the spectacle lenses of a patient with optic atrophy resulting from an accident eliminated constant diplopia in the remaining visual field. A reduction in vision due to Fresnel prisms was found to be more tolerable than diplopia.

Full macular translocation versus photodynamic therapy with verteporfin in the treatment of neovascular age-related macular degeneration: 1-year results of a prospective, controlled, randomised pilot trial (FMT-PDT).

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BACKGROUND The purpose of this study was to compare full macular translocation (FMT) with photodynamic therapy (PDT) in the treatment of neovascular age-related macular degeneration (AMD). METHODS In a prospective, randomised, non-masked, mono-center, pilot-trial, 50 eyes of 50 patients were

Treatment of decompensating strabismic who had diplopia and vertex headaches.

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A 26-year-old female was referred for treatment who presented possible retrobulbar optic atrophy, reduced visual acuity, an LXT, a diplopia, and vertex headaches. Fresnel prisms, the simplest and most logical treatment choice were used to relieve the complaints of diplopia and vertex headaches.

Ocular myasthenia gravis associated with x-linked recessive spinal and bulbar muscular atrophy.

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We describe a 34-year-old patient who was admitted with episodic diplopia, ptosis, and swallowing difficulties of 6 months duration. He also had some muscle cramps aggravated by exercise since the age of 20. Bilateral ptosis of the eyelids, normal gaze, rare fasciculations of the tongue, easy

Myasthenia gravis--a rare presentation with tongue atrophy and fasciculation.

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We report the case of an unusual presentation of myasthenia gravis with tongue atrophy and fasciculation. Myasthenia gravis is an autoimmune condition associated with weakness and fatigability of voluntary muscles. In >50%, the initial symptoms and signs are related to extraocular muscle weakness,

A case of myelopathy, myopathy, peripheral neuropathy and subcortical grey matter degeneration associated with recessive compound heterozygous POLG1 mutations.

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This 54year old woman presented with symptoms of sensory ataxic neuropathy, with cerebellar features. She developed further weakness, visual disturbances with diplopia, dysarthria and dysphasia. After her death at 66years, she was found to have compound heterozygous mutations of POLG1 gene in

Postoperative diplopia and ptosis. A clinical hypothesis based on the myotoxicity of local anesthetics.

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Postoperative diplopia and ptosis can be temporary or permanent complications in patients who have undergone ophthalmic surgery while under local anesthesia. We encountered six patients with such complications and hypothesize that some cases of postoperative diplopia and ptosis could be attributed

[Strabismus and diplopia as complications after cataract surgery with IOL implantation].

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In our Department of Orthoptics we have seen an increasing number of patients suffering from diplopia after cataract surgery with IOL implantation. Between 1993 and 1997 the total number of patients with this problem was 24 (2.7 % of all patients, mean age 71 years, age range 38-88). We addressed

Prevalence of Sagging Eye Syndrome in Adults with Binocular Diplopia.

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Sagging eye syndrome (SES), horizontal and/or vertical strabismus caused by orbital connective tissue degeneration, was first defined 10 years ago. In this study, we investigated the causes of acquired binocular diplopia in adults presenting to single institution since the description

[Paraneoplastic cerebellar degeneration in Hodgkin's disease].

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METHODS A 30-year-old previously healthy man suddenly developed double vision, unsteady gait and some difficulty in speech articulation. Within 4 weeks he had become markedly ataxic, unable to walk, stand or sit down unaided. Neurological examination indicated a severe cerebellar syndrome. There

Voltage-Gated P/Q-Type Calcium Channel Antibodies Associated With Cerebellar Degeneration.

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Paraneoplastic cerebellar degeneration is a rare neurological condition characterized by diffuse cerebellar dysfunction and magnetic resonance imaging evidence of progressive cerebellar atrophy. It has been associated with several autoantibodies and malignancies in adults. To date, only six cases

Progressive solitary sclerosis presented with diplopia: A case report.

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To report a patient presented with diplopia followed by progressive quadriparesis in the setting of a solitary pontomedullary lesion.We report a 24-year-old woman presented with an attack of diplopia with full recovery, followed by progressive

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