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1.
Clin Ophthalmol ; 6: 1619-22, 2012.
Article in English | MEDLINE | ID: mdl-23055687

ABSTRACT

AIM: In this paper, we will try to highlight the importance of various investigations and their crucial role in identifying whether the defect is structural or functional. CASE HISTORY: A 24-year-old woman presented with ocular complications after bungee jumping. Subsequently, although all ophthalmic signs resolved, she complained of decreased vision in her left eye. CONCLUSION: Initial ophthalmic injury was detected by optical coherence tomography scan showing a neurosensory detachment of the fovea. This was not initially detected on slit-lamp examination or fluorescein angiography. On later examination, although the optical coherence tomography scan showed no structural damage, electrodiagnostic tests showed a functional defect at the fovea.

2.
Clin Ophthalmol ; 4: 1211-5, 2010 Oct 21.
Article in English | MEDLINE | ID: mdl-21060674

ABSTRACT

PURPOSE: When investigating a case of unexplained corneal ulceration, we need to think of fungal infection and any predisposing factors. METHODS: A case study of a corneal ulceration in a patient who was HIV positive with a devastating visual outcome. RESULTS: Therapeutic corneal graft was necessary due to corneal perforation. Immunocompromised state of patient was retrospectively diagnosed. CONCLUSIONS: Candida albicans keratitis is an opportunistic infection of a compromised cornea, and sometimes unknowingly compromised host, which can be initially misdiagnosed. Despite intensive antifungal therapy, occasionally patients require corneal grafting to improve vision, and before it is possible to establish an accurate diagnosis.

3.
J Ophthalmol ; 20102010.
Article in English | MEDLINE | ID: mdl-20871658

ABSTRACT

Miller-Fisher syndrome (MFS) is a rare condition characterized by the classical triad of ophthalmoplegia, ataxia, and areflexia (Fisher, 1956). It is considered a variant of Guillain-Barré syndrome (GBS) with which it may overlap, or it can occur in more limited forms. We report a case of a thirty-five-year-old male who presented with a six-day history of diplopia, following a recent chest infection. On examination, he was found to have bilateral sixth nerve palsy, bilateral fourth nerve palsy, bilateral areflexical mydriasis, ataxia and total absence of reflexes. After excluding other conditions, a diagnosis of Miller-Fisher syndrome was made. The patient was administered intravenous immunoglobulin and made an uneventful recovery.

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