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A case of atypical ophthalmoplegia after Chikungunya fever.

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OBJECTIVE This study aims to report an unusual case of bilateral diffuse ophthalmoplegia with levator sparing, in a patient after an episode of Chikungunya fever. METHODS Case report of a five-year-old girl with inability to move both eyes along with decreased near vision. CONCLUSIONS Bilateral

RYR1 mutations as a cause of ophthalmoplegia, facial weakness, and malignant hyperthermia.

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OBJECTIVE Total ophthalmoplegia can result from ryanodine receptor 1 (RYR1) mutations without overt associated skeletal myopathy. Patients carrying RYR1 mutations are at high risk of developing malignant hyperthermia. Ophthalmologists should be familiar with these important clinical

Ophthalmoplegia following enteric fever.

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Double Optic Neuritis and Ophthalmoplegia from Lead Poisoning; Complicated by Typhoid Fever.

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Neurological picture. Internuclear ophthalmoplegia following African tick bite fever.

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Internuclear Ophthalmoplegia as the First Manifestation of Pediatric-Onset Multiple Sclerosis and Concurrent Lyme Disease

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BACKGROUND Internuclear ophthalmoplegia (INO) presents as a disruption of horizontal conjugate ocular movement and is an uncommon finding in the pediatric population. Its presence warrants a thorough evaluation to search for demyelinating, mass effect, inflammatory, or infectious etiologies. CASE

Cryptococcal meningitis and internal ophthalmoplegia.

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A 17-year old girl received prednisone and azathioprine for the treatment of systemic lupus erythematosus. She developed a fever and hallucinations 18 months later; cryptococcal meningitis was diagnosed. An internal ophthalmoplegia with loss of accommodation and dilation of the pupils developed

Cryptococcal meningitis presenting with bilateral complete ophthalmoplegia: a case report.

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BACKGROUND Cryptococcus neoformans is saprophytic encapsulated yeast. Infection is acquired by inhalation of the organism and could be asymptomatic or limited to the lungs, specially in the immunocompetent host. Cryptococcal meningitis is a serious opportunistic infection among post transplant

[Probable Miller Fisher syndrome during Dengue fever type 2].

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A 57 year-old-man developed a left ophthalmoplegia associated with ataxia and areflexia while he had fever (39 degrees C) for two days. Dengue fever (DF) was diagnosed by definite criteria, i.e.: IgM seroconversion, positive culture from serum and positive PCR both from serum and CSF. Within one

Central retinal artery occlusion secondary to dengue fever.

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Dengue fever is endemic in the tropics and subtropics and has become a worldwide health threat in recent years. Dengue-related ocular complications are increasingly being reported from countries in South-East Asia. The authors report the first documented case of a patient with dengue fever who

Miller Fisher syndrome developing as a parainfectious manifestation of dengue fever: a case report and review of the literature.

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Although dengue viral infections have emerged as one of the most important mosquito-borne diseases, neurological manifestations of dengue infections are uncommon. Guillain-Barré syndrome and Miller Fisher syndrome have been reported to occur as immune-mediated complications following

Young adult patient with headache, fever and blurred vision.

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BACKGROUND This case highlights the fact that acute pituitary apoplexy may be misdiagnosed due to being confused with other entities exhibiting similar symptoms, such as meningitis or subarachnoid hemorrhage. METHODS A patient in his late 30s presented with sudden and severe frontal headache, fever,

Ophthalmoplegia Due to Scrub Typhus.

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Scrub typhus is an acute febrile infectious disease caused by Orientia tsutsugamushi. The illness is usually characterized by fever, rash, and lymphadenopathy, but severe cases progress to pulmonary and neurological involvement. We report a 69-year-old man who developed ptosis and ophthalmoplegia

Whipple's disease: multiple hospital admissions of a man with diarrhoea, fever and arthralgia.

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Whipple's disease is a rare chronic multi-systemic infectious disorder caused by the Gram-positive bacillus, Tropheryma whippelii. Infection may involve any organ in the body, and most commonly affects white men in the fourth to sixth decades of life. The most common presenting symptoms are

Familial Mediterranean fever and multiple sclerosis.

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Central nervous system (CNS) manifestations of familial Mediterranean fever (FMF) are extremely rare. These include pseudotumor cerebri, optic neuritis, CNS complications of polyarteritis nodosa type vasculitis, or hypercoagulable states secondary to renal amyloidosis, recurrent aseptic meningitis,

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