![]() 2,3,10 A systemic health history should include questions regarding trauma, diabetes, hypertension, thyroid disease, cancer, infection and immunosuppression-all of which could cause CN palsies and diplopia through vascular or restrictive mechanisms. A thorough systemic health history and step-by-step examination is key to localizing most underlying etiologies. The type of diplopia the patient complains of-horizontal, vertical or diagonal worse at distance or near increased or decreased in a particular gaze position-helps to identify which extraocular muscle is involved. ![]() Unlike monocular diplopia, binocular diplopia, due to ocular misalignment, will disappear when either eye is covered. 9Īs many as 60% of MG patients, such as this one, present with ptosis and diplopia. 4,7,8 Medications (e.g., antidepressants, antihistamines, diuretics) may contribute to ocular surface dryness and induce a monocular diplopia. Decreased vision due to uncorrected astigmatism, dry eye and tear film deficiencies, corneal pathology or scarring, iris abnormalities, lenticular changes, vitreal opacities and macular disease are all possible causes of monocular diplopia. This finding is rarely due to cortex lesion and is generally attributable to causes within the eye itself. Clinicians should have the patient cover each eye separately when testing for monocular diplopia. 3,4 Monocular Diplopiaĭiplopia that persists when one eye is covered falls into the category of monocular diplopia, or polyopia (greater than two images). The clinician must determine if the diplopia is monocular or binocular, as binocular diplopia may have a life-threatening cause. The first step on the path to proper identification is a thorough patient history. 6 A systematic approach to the differentials is key to identifying and treating benign causes-and promptly referring patients when it is vision or life threatening.ĬN VI palsy, seen here in the right eye, accounts for 50% of all isolated CN palsies. 4,5 Most etiologies will fall into one of five categories: (1) refractive, (2) binocular vision disorder, (3) orbital disease, (4) neuromuscular junction dysfunction, or (5) injury to the central nervous system/cranial nerves (CNs). 2,3 While the cause can be benign, some cases, such as those accompanied by new headache, ocular pain, unilateral pupil dilation, muscle weakness, ptosis, trauma or papilledema, raise red flags for immediate referral. 1 Constant diplopia with acute onset will have different differentials than intermittent diplopia, for example. 1965 10: 129-85.A patient presenting with diplopia-whether horizontal, vertical or diagonal-is often a clinical challenge. Pupillotonic Pseudotabes (Syndrome of Markus-Weill and Reys-Holmes-Adie): A Critical Review of the Literature. Tonic pupils and absent tendon reflexes: a benign disorder sui generis its complete and incomplete forms. Argyll Robertson pupils true and false Br Med J. A benign disorder simulating tabes dorsalis. Pseudo-Argyll Robertson pupils with absent tendon reflexes. Partial iridoplegia associated with symptoms of other diseases in the nervous system. A propos d’un cas de réaction tonique d’une pupille a la convergence et parésie de l’accommodation avec aréflexie a la lumière chez un sujet atteint de crises tétaniformes et d’aréflexie des membres inférieurs. Klinische Monatsblätter für Augenheilkunde. Über die beziechung “myotonische Pupillenbewegung”. Über die sogenannte “myotonische” Convergenzträgheit lichstarrer Pupillen. In: Transactions of the Ophthalmological Societies of the United Kingdom, 1881, 1: 139-154. Philosophical Transactions of the Royal Society of London, 1813: 103: 31–50. Observations relative to the near and distant sight of different persons.
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