You searched for "misdiagnosis"
A case of post-viral ocular microflutter
1 August 2018
| Claire Howard
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EYE - Neuro-ophthalmology
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Ocular flutter, ocular microflutter, opsoclonus, saccadic intrusions, video-oculography
A number of eye movements disrupt visual fixation, one such movement being saccadic intrusions which are described as small involuntary saccadic movements. Among saccadic intrusions without intersaccadic intervals, ocular flutter and opsoclonus are prominent. When the saccadic amplitude is very...
CSD-OCT detection of minimally visible retinoblastoma
This paper reports minimally visible tumour recurrence that was detectable on spectral domain OCT (SD-OCT) in a two-month-old infant who had a diagnosis of bilateral familial retinoblastoma. The infant was treated with IVC for six cycles with vincristine, etoposide and...IOL cataract surgery 7-24 months
The purpose of this study was to present the long-term outcome of IOLs in paediatric patients who received cataract surgery aged seven to <24 months. This was retrospective study with minimum follow-up of 12 months for 27 patients (28 eyes)....International variations in ROP treatment
1 August 2018
| Jonathan Chan
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EYE - Vitreo-Retinal
A retrospective cohort review of 48,087 premature infants weighing <1500 gm between 24 to 27 weeks gestation, from 11 high income countries in Australia, New Zealand, Canada, Finland, Israel, Japan, Spain, Sweden, Switzerland, Tuscany (Italy) and the UK . By...
Identification and diagnosis of thalamic haemorrhage
1 August 2014
| Claire Howard
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EYE - Neuro-ophthalmology
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Eye movements, neuro-ophthalmology, thalamic haemorrhage
This paper presents a case of thalamic haemorrhage and discusses clinical findings, providing valuable insight into signs clinicians need to look for. The case presented is of a 76-year-old female who developed left hemiplegia and hemi anaesthesia. Ocular motility testing...
An unusual case of sellar chondroma
1 June 2014
| Claire Howard
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EYE - Neuro-ophthalmology
A single case of chondrogenic neoplasm arising from the base of the skull is presented and discussed. These benign and slow growing tumours in the sellar region are extremely rare and as such this article provides a useful insight and...
Arterial stiffness and PEX
1 April 2014
| Lorraine North
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EYE - Glaucoma
The authors describe a study of 25 newly diagnosed patients with pseudoexfoliation glaucoma (PEX) and 25 controls to evaluate carotid femoral pulse wave velocity (CF-PWV) values. The CF-PWV was assessed using a noninvasive device by measuring the pulse transmit time...
Clinical and neuro-ophthalmologic predictors of visual outcome in idiopathic intracranial hypertension
1 October 2018
| Claire Howard
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EYE - Neuro-ophthalmology
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Idiopathic intracranial hypertension, predictors, visual outcome
This prospective study of 40 patients aims to assess visual morbidity in patients with idiopathic intracranial hypertension (IIH). Final visual outcome of patients was compared with clinical and neuro-ophthalmic parameters such as visual acuity, visual field, contrast sensitivity, retinal nerve...
Repeated ptosis surgery
The purpose of this study was to evaluate the amounts of surgery for the treatment of residual or recurrent simple congenital ptosis and to investigate the relationship between long-term surgical success rates with clinical and surgical factors. This was a...Association between neuro-ophthalmology signs and chronic ataxia in children
1 October 2015
| Claire Howard
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EYE - Neuro-ophthalmology
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Chronic ataxia, neuro-ophthalmology, paediatrics
Neuro-ophthalmological signs (N-OS) occur commonly in children with chronic ataxia. This study describes the N-OS and their frequencies, in general and by specific disease aetiology in paediatric patients with chronic ataxia. In total, 184 patients under the age of 17...
Differential diagnosis of inflammatory optic neuritis
1 February 2014
| Claire Howard
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EYE - Neuro-ophthalmology
The authors present the differential diagnosis of inflammatory optic neuritis (ON) to include multiple sclerosis, infectious optic neuritis, systemic disease and neuromyelitis optica (NMO). The features of ON for the varying aetiologies are detailed including incidence and overlap. In acute...
Molecular genetics of achromatopsia
1 December 2013
| Nana Theodorou
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EYE - Vitreo-Retinal
Achromatopsia is a rare autosomal recessive disorder of the cone photoreceptors. Typical characteristics of affected patients include the inability to distinguish colours, impaired visual acuity, photophobia and nystagmus. The condition is said to be more frequent in the Pingelapese population...