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   Table of Contents      
Year : 2009  |  Volume : 57  |  Issue : 6  |  Page : 463-464

Botulinum toxin in the management of acquired motor fusion deficiency

1 Department of Pediatric Ophthalmology and Strabismus, and Oculoplasty, Orbital diseases and Ocular Oncology, LV Prasad Eye Institute, Hyderabad, India
2 Department of Pediatric Ophthalmology and Strabismus, LV Prasad Eye Institute, Hyderabad, India

Date of Submission26-Jul-2008
Date of Acceptance08-Dec-2008
Date of Web Publication21-Oct-2009

Correspondence Address:
Ramesh Murthy
Pediatric Ophthalmology and Strabismus, Oculoplasty and Ocular Oncology, LV Prasad Eye Institute, Kallam Anji Reddy Campus, LV Prasad Marg, Banjara Hills, Hyderabad- 500 034
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0301-4738.57162

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Acquired disruption of motor fusion is a rare condition characterized by intractable diplopia. Management of these patients is extremely difficult. Prisms in any combination or even surgery may not help relieve their symptoms. We describe a longstanding case of acquired motor fusion disruption which was managed successfully with botulinum toxin injection.

Keywords: Acquired motor fusion deficiency, botulinum toxin

How to cite this article:
Murthy R, Kesarwani S. Botulinum toxin in the management of acquired motor fusion deficiency. Indian J Ophthalmol 2009;57:463-4

How to cite this URL:
Murthy R, Kesarwani S. Botulinum toxin in the management of acquired motor fusion deficiency. Indian J Ophthalmol [serial online] 2009 [cited 2023 Dec 1];57:463-4. Available from: https://journals.lww.com/ijo/pages/default.aspx/text.asp?2009/57/6/463/57162

Acquired disruption of motor fusion is characterized by diplopia in all positions of gaze and is associated with strabismus. [1] It can occur following prolonged sensory deprivation in one eye as can occur when a previously normal eye has an untreated monocular cataract for a prolonged period or sometimes even after cataract extraction. [1],[2] It can occur after severe head injury, postviral syndromes or with other central nervous system disorders. [1] Patients with this disorder experience constant diplopia that cannot be eliminated with prisms. As they have lost central fusional abilities they can neither fuse nor suppress the images. In this report we describe a patient who developed acquired motor fusion deficiency which was managed by botulinum toxin injection with a successful outcome.

  Case Report Top

A 30-year-old lady presented to the squint clinic with complaints of constant diplopia and outward deviation of the right eye following head trauma three years back in a road accident. Prior to the accident, she had never had diplopia or squinting of the eyes. She had developed bilateral sensorineural hearing loss following the accident. Computed tomography (CT) scan had revealed a subdural hematoma in the right frontal region which had been managed conservatively and had resolved. On examination her visual acuity was 20/20 for distance and N6 for near in each eye. Anterior segment and fundus examination was within normal limits. There was no sign of any macular disease on fundus examination. Cover testing revealed a freely alternating exodeviation of 40 prism dioptres (PD) for near and distance [Figure 1]. Convergence could not be demonstrated. Ductions were full in all gazes. Diplopia charting revealed binocular crossed diplopia with constant separation of images in all gazes. There was no indication of torsional abnormality on diplopia testing. Humphrey visual field testing did not reveal any field loss. Fusion was not possible in free space with any combination of prisms even after prolonged prism adaptation in the clinic on two consequent visits. Based on this a diagnosis of acquired motor fusion deficiency was made. She was administered botulinum toxin injection (Botox, Allergan Inc) 2.5 units into each lateral rectus muscle under electromyographic guidance. Review at the end of one month revealed a reduction in the exotropia to 10 PD and subjective appreciation of closeness of the two images. She was subsequently administered a repeat injection of 2.5 units of botulinum toxin into the left lateral rectus muscle. Follow-up after one month revealed complete resolution of the diplopia. There was no abnormal head posture. Objective examination revealed she was orthophoric for near and exophoric for distance and extraocular movements were full. Follow-up six months later revealed she was completely symptom-free. There was no exotropia on cover test [Figure 2]. The horizontal fusion ranges were 30 PD base out and 16 PD base in for near and 16 PD base out and 8 PD base in for distance. The vertical fusion range was 3 PD base up and 3 PD base down. She demonstrated gross stereopsis on the Wirt fly test.

  Discussion Top

Acquired strabismus occurring after visual maturation results in diplopia. In most cases the ability to fuse allows the patients to regain binocular single vision when the misalignment is eliminated. [3],[4] However, in patients with central disruption of fusional amplitude, the ability to superimpose the images may be completely lost. This results in constant diplopia which can be eliminated only by occluding one eye. [5] A diagnosis of central disruption of fusion should not be made unless all other causes for intractable diplopia have been excluded, including torsion and aniseikonia. [1],[6] Prolonged prism adaptation or testing on a synoptophore is essential before making this diagnosis.

Strabismus is common after head trauma, even if the brainstem is not obviously affected. The strabismus may be due to paresis of one or more cranial nerves, diffuse brain damage or due to central disruption of fusional amplitudes because of damage to the vergence centers of the midbrain. [2] Sometimes the brain may simply lose its ability to fuse because of prolonged deprivation of fusable images. [2] Pratt-Johnson hypothesized that midbrain damage may be a cause for the disruption of convergence and or divergence, leading to inability to fuse. [5] Orthoptic treatment has been reported to be effective in patients where there is a diminished fusional range without a complete loss of fusion. [7] However, this may not happen in cases where there is no demonstrable fusion.

Consequently, if the lack of fusable images can lead to disruption of central fusion as following prolonged occlusion due to cataract, presence of fusable images may aid in recovery from central fusion disruption. In our patient botulinum toxin injections helped to align the eyes for prolonged periods thereby presenting continuous fusable images to the brain. This may have facilitated recovery from the diplopia which may or may not have resolved otherwise. Botulinum toxin is a minimally invasive, quick outpatient procedure and can be repeated. Botulinum toxin may be worth attempting in patients with intractable diplopia following central fusion disruption.

  References Top

Benegas NM, Egbert J, Engel WK, Kushner BJ. Diplopia secondary to aniseikonia associated with macular disease. Arch Ophthamol 1999;17:896-9.  Back to cited text no. 1
Sharkey JA, Sellar PW. Acquired central fusion disruption following cataract extraction. J Pediatr Ophthalmol Strabismus 1994;31:391-3.  Back to cited text no. 2
Fowler MS, Wade DT, Richardson AJ, Stein JF. Squints and diplopia seen after brain damage. J Neurol 1996;243:86-90.  Back to cited text no. 3
Rutstein RP, Bessant B. Horror fusionis: a report of five patients. J Am Optom Assoc 1996;67:733-9.  Back to cited text no. 4
Pratt-Johnson JA, Tillson G. Acquired central disruption of fusional amplitude. Ophthalmology 1979;86:2140-2.  Back to cited text no. 5
Kushner BJ. Unexpected cyclotorsion simulating disruption of fusion. Arch Ophthalmol 1992;110:415-8.  Back to cited text no. 6
Stanworth A. Defects of ocular movement and fusion after head injury. Br J Ophthalmol 1974;58:266.  Back to cited text no. 7


  [Figure 1], [Figure 2]

This article has been cited by
1 Botulinum toxin in the management of acquired motor fusion deficiency: The missing links
Pandey, P.K., Dadeya, S., Vats, P., Singh, A., Rathi, N., Dangda, S.
Indian Journal of Ophthalmology. 2010; 58(5): 446
2 Authorsę reply
Murthy, R., Kesarwani, S.
Indian Journal of Ophthalmology. 2010; 58(5): 446-447


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