Intermittent diplopia: a practical guide

Intermittent binocular diplopia is challenging to assess, as symptoms may be absent during examination yet its possible causes range from benign decompensation to serious disease. We outline a practical method to evaluate intermittent diplopia, focusing on four key steps: (1) confirming binocular diplopia, (2) assessing monocular ductions to detect paretic or restrictive deficits, (3) determining comitance (whether the angle of strabismus is equal in all directions of gaze) to distinguish fusional from neurological or orbital causes and (4) evaluating fatigability to identify ocular myasthenia. We emphasise clinical scenarios requiring targeted testing, including giant cell arteritis and malignancy and discuss when orthoptic or ophthalmic referral is more appropriate than extensive neurological investigation. We also describe recognisable neurological entities such as ocular neuromyotonia and superior oblique myokymia. We aim to provide clinicians with an efficient method to assess intermittent diplopia, avoid unnecessary investigations and ensure that important pathology is not missed.

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Publication Details

Journal
Practical Neurology
Published
2026-04-30
DOI
https://doi.org/10.1136/pn-2026-005132
Primary Topic
Ophthalmology and Eye Disorders
Type
article
Field-Weighted Citation Impact
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article

Intermittent diplopia: a practical guide

Wilco Perini, Laurentius J. van Rijn, A van den Berg, Sunjay Parmar et al.
Practical Neurology
Ophthalmology and Eye Disorders
article

Intermittent diplopia: a practical guide

Wilco Perini, Laurentius J. van Rijn, A van den Berg, Sunjay Parmar, Axel Petzold, Vincent J.J. Odekerken, Susan P Mollan, Veron Verhorst
article en

Abstract

Intermittent binocular diplopia is challenging to assess, as symptoms may be absent during examination yet its possible causes range from benign decompensation to serious disease. We outline a practical method to evaluate intermittent diplopia, focusing on four key steps: (1) confirming binocular diplopia, (2) assessing monocular ductions to detect paretic or restrictive deficits, (3) determining comitance (whether the angle of strabismus is equal in all directions of gaze) to distinguish fusional from neurological or orbital causes and (4) evaluating fatigability to identify ocular myasthenia. We emphasise clinical scenarios requiring targeted testing, including giant cell arteritis and malignancy and discuss when orthoptic or ophthalmic referral is more appropriate than extensive neurological investigation. We also describe recognisable neurological entities such as ocular neuromyotonia and superior oblique myokymia. We aim to provide clinicians with an efficient method to assess intermittent diplopia, avoid unnecessary investigations and ensure that important pathology is not missed.

Practical Neurology
Moorfields Eye Hospital NHS Foundation Trust (GB), Guy's and St Thomas' NHS Foundation Trust (GB), Queen's University (CA), OLVG (NL), Amsterdam Neuroscience (NL), Birmingham Dental Hospital (GB), Moorfields Eye Hospital (GB), National Hospital for Neurology and Neurosurgery (GB), University College London (GB), University of Birmingham (GB)
Good health and well-being
Openalex Percentile: Top 12%
Ophthalmology and Eye Disorders
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