Esotropia

From EyeWiki
Original article contributed by: Dimitra Triantafilou, CO, Donny W. Suh, MD,FAAP
All contributors: A. Paula Grigorian, MD and Donny W. Suh, MD,FAAP
Assigned editor:
Review: Assigned status Update Pending by A. Paula Grigorian, MD on January 22, 2015.



Esotropia
Classification and external resources
ICD-10 H50.0
DiseasesDB 29856


Disease Entity[edit | edit source]

Strabismus/Ocular misalignment

Disease[edit | edit source]

Esotropia is an eye misalignment in which one eye is deviated inward, or nasally. The deviation may be constant or intermittent. The deviating eye may always be the same eye or may alternate between the two eyes.

Types[edit | edit source]

Infantile esotropia[edit | edit source]

This is an esodeviation, often constant, that presents in the first 12 months of life. It is associated with a large angle deviation, latent nystagmus, a crossfixation pattern of fixation, a normal accommodative convergence to accommodation ratio, and age-appropriate refractive errors.

Accommodative esotropia[edit | edit source]

This esotropia is associated with an onset after 1 year of age. They often have a gradual onset and may evolve to becoming constant after a period of intermittency. Fully accommodative esotropia is associated with high hyperopia of +3.00 D or greater and inadequate fusional divergence amplitudes.

A subtype of accommodative esotropia is convergence excess type esotropia, which is associated with a deviation greater at near than distance. The deviation at near is reduced when accommodation is relaxed with +3.00D lenses. The mechanism is an abnormal ratio between accommodative convergence and accommodation (high accommodative convergence to accommodation ratio); the effort to accommodate elicits an abnormally high accommodative convergence response. Partially accommodative esotropia is a residual esotropia that is partially corrected, yet still persists in spite of full correction of hyperopic refractive error.

Non-accommodative esotropia[edit | edit source]

This esodeviation has an onset after 1 year of age, and is not associated with any accommodative factor.

Divergence insufficiency type esotropia[edit | edit source]

This esotropia, most often associated with adult patients 30 years and older, is characterized by an esodeviation greater at distance than near. Fusional divergence amplitudes are reduced at both distance and near fixation, and this esotropia is comitant in primary and lateral gazes.

Microtropia/Monofixation Syndrome[edit | edit source]

This is characterized by patients with a central scotoma in one eye together with peripheral fusion. These patients typically lack fine stereopsis and maintain a mild to moderate degree of fusional amplitudes.

Sensory esotropia[edit | edit source]

Unilateral reduced visual acuity, due to various organic causes, presents a barrier to fusion. In children under 4 years of age, the blind or poorer-seeing eye will generally become esotropic. Older children or adults with sensory visual deprivation will generally develop a sensory exotropia.

Consecutive esotropia[edit | edit source]

This occurs when a person who was formerly exotropic becomes esotropic. Sometimes this is a result of surgical overcorrection for exotropia.

Etiology[edit | edit source]

The etiology of esotropia is unknown in most cases, but it can be hereditary. Sensory esotropia occurs because of decreased acuity in one eye, due to various organic causes, which leads to an inability to maintain normal eye alignment. It is thought that strabismus occurs because of a problem with the fusional system.

Risk Factors[edit | edit source]

Neurological disorders, hydrocephalus, prematurity, and a positive family history of strabismus increase the risk of having esotropia.

General Pathology[edit | edit source]

Accommodative esotropia is the most common subtype of esotropia, with an onset after 1 year of age and usually detected around 2-3 years of age. There is no predilection for esotropia in terms of age or gender.


Physical examination[edit | edit source]

All patients with esotropia would need a complete ophthalmologic examination, including visual acuity, binocular function and stereopsis, motility evaluation, strabismus measurements at near, distance, and cardinal positions of gaze, measurement of fusional amplitudes, cycloplegic refraction. Some cases may require a 4 prism diopter base out test for microtropia, strabismus measurements after Marlowe’s prolonged occlusion test, strabismus measurements after +3.00 lenses at near fixation, evaluation of ocular structures in the anterior and posterior segments.


Symptoms[edit | edit source]

Symptoms are quite variable in terms of frequency and severity of the esotropia. If a child suppresses the deviated eye, the patient can develop an amblyopia or a more severe angle or frequency of the strabismus. Adults with esotropia may experience diplopia.

Clinical diagnosis[edit | edit source]

Infantile esotropia[edit | edit source]

An infant with an esotropia that is usually constant and presents within the first one year of life. It is associated with a large angle deviation, latent nystagmus, crossfixation, a normal accommodative convergence to accommodation ratio, and age-appropriate refractive errors.

Accommodative esotropia[edit | edit source]

Occurs in children over 1 year of age. In general, this is associated with hyperopia which reduces the angle and/or frequency of the esotropia when the hyperopic correction is worn. Accommodative esotropia may also be associated with microtropia/monofixation syndrome.

Non-accommodative esotropia[edit | edit source]

This subtype has an onset after 1 year of age, can be constant or intermittent, and is not affected by the level of accommodation.

Divergence insufficiency type esotropia[edit | edit source]

This type of esotropia is found in the population 30 years of age and above. These patients have reduced fusional divergence amplitudes, the esotropia is worse at distance than near, and they may have trouble with driving or diplopia with distance fixation.

Microtropia/Monofixation Syndrome[edit | edit source]

This is characterized by patients with a central scotoma in one eye together with peripheral fusion, fusional amplitudes, and gross stereopsis.

Differential diagnosis[edit | edit source]

Other conditions that can display esotropia include Duane Syndrome types 1 or 3, 6th CN palsy, Nystagmus blockage syndrome, Moebius syndrome, thyroid eye disease, Myasthenia gravis, congenital fibrosis of the extraocular muscles, slipped lateral rectus muscle, or tight medial rectus muscle.

Management[edit | edit source]

Nonsurgical[edit | edit source]

Nonsurgical treatments include patching, correction of full hyperopic refractive error, and divergence orthoptic exercises for divergence insufficiency. Fresnel prisms or prism glasses can be used to relieve diplopia or asthenopia in certain patients. Sometimes sensory esotropia can be helped by treating the underlying cause (amblyopia, cataract, media opacity).

Surgery[edit | edit source]

Surgery is performed on the extraocular muscles in an attempt to give binocular single vision, to relieve diplopia, or to restore the eyes to their regular state of alignment. The prognosis for surgical success is best if the patient has an intermittent esotropia rather than a constant one, and alternating esotropia, and if any amblyopia is treated. In certain cases, amblyopia may not be fully corrected due to the strabismus, and surgery may be needed prior to full correction of the amblyopia. The optimal time for surgical intervention is as early as possible prior to any degenerations of the lateral geniculate nucleus. Studies have shown that surgeries as early as six months of age can be effective.

References[edit | edit source]

  1. Baker JD, Parks MM. Early onset accommodative esotropia. Am J Ophthalmol 1980: 90:11.
  2. Cassin B, Beecham B, Friedberg K. Stereoacuity, fusional amplitudes and AC/A ratio in accommodative esotropia. Am Orthopt J 1976; 26:60-64.
  3. Costenbader F. Infantile esotropia clinical characteristics and diagnosis. Am Orthopt J 1968; 18:5-10.
  4. Foster RS, Paul O, Jampolsky A. Management of infantile esotropia. Amer J Ophthalmol 1974; 82:291-299.
  5. Helveston E. Origins of congenital esotropia. Am Orthopt J. 1986; 36:40-48.
  6. Ing MR. Early surgical alignment for congenital esotropia. J Ped Ophthalmol Strab 1984; 20:11-18.