Abducens Nerve Palsy

From EyeWiki

Abducens Nerve Palsy

Disease Entity

Strabismus/ocular misalignment


Abducens (sixth cranial) nerve palsy is the most common ocular motor paralysis in adults and the second-most common in children. The abducens nerve controls the lateral rectus muscle, which abducts the eye. Abducens nerve palsy causes an esotropia due to the unopposed action of the antagonistic medial rectus muscle. The affected eye turns medially and is unable to abduct properly. The esodeviation is incomitant, greater when the patient is looking toward the affected side and when fixating at distance versus at near.


Damage or disruption to the abducens nerve anywhere along its long intracranial course can result in a palsy. The abducens nerve has the longest intracranial course of all the cranial nerves. The nerve begins at its nucleus in the dorsal pons and courses superiorly and then anteriorly before leaving the brainstem at the pontomedullary junction. It then travels along the skull base in the subarachnoid space, over the petrous apex of the temporal bone tethered in Dorello’s canal (i.e. an opening below the petroclinoid ligament) and through the cavernous sinus and superior orbital fissure and enters the orbit, traveling through the annulus of Zinn to reach the lateral rectus muscle. Potential etiologies of abducens nerve palsy are different in children and adults and depend on the anatomic location of damage.

In pediatrics

  • Congenital.
    • Congenital palsies are relatively rare. They can be associated with birth trauma, developmental neuronal migration defects,[1] and with neurological conditions such as hydrocephalus and cerebral palsy.
  • Acquired.
    • Acquired abducens nerve palsies in childhood can be due to neoplasm, trauma, infection, inflammation, and idiopathic etiologies. Non-traumatic acquired sixth nerve palsies may be due to benign recurrent sixth nerve palsy, pontine gliomas, elevated or low intracranial pressure, and in rare cases, acute lymphoblastic leukemia.[2] Benign isolated abducens nerve palsy can occur in childhood during an episode of sinusitis,[2] or following an ear, throat, or viral infection. Rarely, isolated abducens nerve palsy can present in children with Kawasaki disease after IVIG therapy.[3]
  • Intracranial tumor.
    • Brainstem gliomas are one of the common tumors seen in the pediatric population, and more than 80% arise from the pons with the peak age of onset between 5-8 years of age. Presenting symptoms include ataxia, disturbance of gait, and unilateral or bilateral abducens nerve palsy.
    • Posterior fossa tumors, such as pontine gliomas, medulloblastomas, ependymomas, trigeminal schwannomas,[4] or cystic cerebellar astrocytomas can produce unilateral or bilateral abducens nerve palsies in children. Abducens nerve palsy can also present as a postoperative complication after resection of posterior fossa tumors in the pediatric population.
  • Trauma, secondary to open or closed head injuries
    • Trauma causes indirect pressure on the nerve, which is very susceptible to trauma as it passes over the apex of the petrous portion of the temporal bone to the cavernous sinus. In addition, traumatic abducens nerve palsy can occur secondary to bruising and/or hemorrhage causing pressure on the nerve. Closed head trauma may cause elevated intracranial pressure (ICP) and secondarily produce a non-localizing sixth nerve palsy.
  • Elevated or low intracranial pressure
    • Elevated intracranial pressure can cause stretching of the sixth cranial nerves which are tethered in Dorello’s canal. The same mechanism can explain the reason for the non-localizing sixth nerve palsy that can be seen with either elevated or reduced intracranial pressures.[5] Elevated intracranial pressure can occur secondary to a variety of different causes, including shunt failure, idiopathic intracranial hypertension, posterior fossa tumors, neurosurgical trauma, venous sinus thrombosis, meningitis, or Lyme disease.
  • Meningitis
    • Hanna et al found abducens nerve palsy in 16.5% of patients with acute bacterial meningitis. Cranial nerve palsies in this setting tend to be multiple and bilateral.[6]

Based on an retrospective study of 14 patients admitted to Hacettepe University Children’s Hospital Pediatric Emergency Department between Jan 01, 2002 and December 31, 2012.[2]

In adults

  • Microvascular ischemia
  • Trauma
  • Idiopathic
  • Less likely:
    • Multiple sclerosis
    • Neoplasm (Skull base tumors-Clivus (meningioma, chordoma, nasopharyngeal carcinoma, metastasis) predominate in the adult population)
    • Stroke
    • Sarcoidosis/vasculitis
    • Increased intracranial pressure
    • Giant cell arteritis
    • Hypophosphatasia Syndrome (with secondary clival thickening)[7]
    • Gestational Hypertension[8]
    • Gradenigo syndrome[9]
    • Creutzfeldt-Jakob Disease[10]
    • Syphilis[11]
    • Poliomyelitis[11]
    • Mastoiditis[11]
    • COVID [12]
  • Lesions causing abducens nerve palsy can also be classified by the location of the lesion.
    • Fascicular
      • Demyelination, vascular disease, and metastatic tumors are likely causes of fascicular damage. Lesions in this area can cause Foville’s syndrome (damage to the pontine tegmentum) which is classified by partial sixth nerve palsy, ipsilateral facial weakness, loss of taste in the anterior portion of the tongue, ipsilateral Horner’s syndrome, ipsilateral facial sensory loss and ipsilateral peripheral deafness. Lesions in the fascicular area can also cause Millard-Gubler syndrome, which is a result of damage to the ventral pons, is characterized by sixth nerve palsy and contralateral hemiplegia, and may or may not also have ipsilateral facial paralysis.
    • Peripheral
      • Causes of peripheral nerve damage include closed head injury, compression, and bacterial infection of the inner ear. Localized compression can be caused by a primary pituitary tumor, craniopharyngioma, schwannoma,[13] or meningioma. Metastatic tumors and aneurysms involving the basilar artery can also cause an abducens nerve palsy.
Based on a retrospective study reported by the Mayo Clinic from 1950’s to 1980’s for patients of all age groups (1919 patients total)[11]

Risk Factors

Inflammatory and microvascular conditions are risk factors for abducens nerve palsy. Other risk factors include multiple sclerosis, encephalitis, meningitis, cavernous sinus thrombosis, hypertension, hypercholesterolemia, aneurysm, diabetes, arteriosclerosis, birth trauma, and neurosurgical intervention.[11]



The pattern of onset and associated symptoms can be very important in determining the etiology of an abducens nerve palsy. Sudden onset suggests a vascular etiology, while slowly progressive onset suggests a compressive etiology. Subacute onset suggests a demyelinating process.

Physical examination

All patients with presumed abducens nerve palsy need a complete ophthalmologic examination, including visual acuity, binocular function and stereopsis, motility evaluation, strabismus measurements at near, distance, and in the cardinal positions of gaze, measurement of fusional amplitudes, cycloplegic refraction, and evaluation of ocular structures in the anterior and posterior segments. Precise assessment of ductions and versions, as well as precise orthoptic measurements in lateral gazes are helpful in determining incomitance associated with abducens nerve palsy. Slow saccadic velocity in side gaze may be present and is helpful with the diagnosis. In children, given that neoplasms and trauma are the most common etiologies of abducens nerve palsy, immediate and careful evaluations must be performed to rule out serious etiologies.[2] It is important to keep in mind the pseudo-restrictive effects of alternating monocular fixation and vergence when having both eyes open at the same time; therefore, each eye must be tested independently.[11]


The cardinal sign of abducens nerve palsy is esotropia of the affected eye due to unopposed action of the medial rectus muscle. The esotropia is incomitant; it is greater on attempted abduction of the affected eye and on distance fixation. Because the greatest motility deficit occurs on an attempt to abduct the affected eye, palpebral fissure widening upon abduction may be seen with maximal abduction effort. The patient may also present with a head turn toward the affected eye, to avoid abduction and thereby minimize diplopia.[14] It is important to differentiate isolated sixth nerve associated abduction deficit from a gaze palsy or INO as this would localize the lesion to the nucleus/internuclei of the 6th and 3rd nerves, respectively.[15]


Diplopia is the most common presenting symptom. Patients will have horizontal uncrossed diplopia which is greater at distance than at near. The diplopia is also worse in the direction of the palsied muscle and gets better in the contralateral gaze. In recent onset palsies, the deviation measures greater when the paretic eye is fixating and smaller when the nonparetic eye is fixing (primary and secondary deviations, respecting Hering's law).

Other symptoms associated with abducens nerve palsy depend on the underlying etiology. In cases due to raised intracranial pressure, patients may experience associated symptoms of headache, pain around the eyes, nausea, vomiting, or pulse synchronous tinnitus. Low ICP from a CSF leak can also cause abducens palsy and can present with symptoms of headache and can hence present clinically very similarly to raised ICP.[5] If a patient has a lesion causing the abducens nerve palsy which affects other structures in the brain, other neurologic signs may be observed.[16] In the event of subarachnoid hemorrhage, the patients can present with leptomeningeal irritation and present with cranial nerve palsies.[17]

If the etiology of the abducens nerve palsy is a brainstem lesion affecting the sixth cranial nerve fasciculus, there may be associated ipsilateral facial weakness, contralateral hemiparesis, or sensory abnormalities (Millard-Gubler syndrome). If the abducens nerve palsy presents together with other ipsilateral cranial nerve palsies, etiology could be a lesion involving the meninges, superior orbital fissure, orbital apex, or cavernous sinus.

Clinical diagnosis

The diagnosis of abducens nerve palsy is usually made on clinical examination. On exam, there is inability to abduct the affected eye. Abducens nerve palsy causes an incomitant esotropia due to the unopposed action of the antagonistic medial rectus muscle. The affected eye turns in toward the nose and is unable to abduct properly. The deviation is usually greater at distance fixation than at near, and also greater on attempted abduction of the affected eye.

Diagnostic procedures

After clinical examination, the most common diagnostic procedure is brain and orbital magnetic resonance imaging (MRI) with gadolinium and fat suppression. MRI can be especially useful in localizing abducens nerve lesions and ruling out serious underlying etiologies, especially neoplasm. Additionally, MRI of the brain and orbits can sometimes help distinguish between high and low ICP.

MRI is recommended in all patients under the age of 50 years, those that present with non-isolated abducens nerve palsy, have a history of cancer, or have an absence of microvascular risk factors. However, controversy remains regarding the importance of MRI in elderly patients with isolated abducens nerve palsy and vasculopathic risk factors. A prospective study found an etiology other than ischemia in 16.5% of such patients.[18] These included giant cell arteritis, brainstem infarction, petroclival meningioma, and cavernous sinus B cell lymphoma. Due to the possibility of dangerous diseases presenting with an isolated cranial motor neuropathy, the authors recommended MR imaging even if a microvascular cause is suspected.[18] However, a cost-effectiveness study found relatively low diagnostic yield for MRI imaging in these patients and concluded that it may not be medically necessary to perform MRI on every patient with an isolated cranial nerve palsy.[19]

Laboratory test

  • Complete blood cell (CBC) count
  • Glucose levels
  • Glycosylated hemoglobin (HbA1C)
  • Erythrocyte sedimentation rate
  • C-reactive protein
  • Fluorescent treponemal antibody-absorption test, VDRL or RPR
  • Lyme titer
  • Glucose tolerance test
  • Antinuclear antibody test
  • Rheumatoid Factor test
  • Angiotensin-converting enzyme (ACE)
  • Magnetic resonance imaging (MRI) could be performed for the following:
    • Patients younger than 50 years
    • Associated pain or other neurologic abnormality
    • History of cancer
    • Bilateral sixth nerve palsy
    • Optic nerve edema
    • If no marked improvement is seen after 3 months or other nerves become involved
  • Lumbar puncture can be considered if MRI results are negative.

Differential diagnosis

Differential diagnosis for abducens nerve palsy includes:

  • Vasculopathy: Hypertension, Diabetes mellitus, aneurysm
  • Congenital: Duane retraction syndrome (Types 1 and 3), essential infantile esotropia
  • Infectious/Inflammatory: Sphenoiditis, lateral rectus myositis.
  • Autoimmune/Inflammatory: Myasthenia gravis, Miller-Fisher syndrome, thyroid eye disease
  • Neoplastic[20]
  • Traumatic: Blowout fracture with entrapment of the medial rectus
  • Other: Spasm of the near reflex, longstanding esotropia with medial rectus contracture, ocular neuromyotonia

Duane syndrome may be differentiated from an abducens nerve palsy by the presence of narrowing of the lid fissure in adduction, which may be seen in Duane syndrome but not in an abducens nerve palsy.

Thyroid eye disease, although more commonly bilateral, may present with unilateral symptoms including proptosis and symptoms of inflammation upon awakening.[11]

Diplopia in myasthenia gravis fluctuates and is fatigable and with or without generalized fatigability, shortness of breath and hoarseness.[11]

Clinical assessment for orbital, neuromuscular, and brainstem disease is the first step in evaluation for this condition, and after this, an abducens nerve palsy can be diagnosed by exclusion.


General treatment

Treatment of abducens nerve palsy depends on the underlying etiology. In general, underlying or systemic conditions are treated primarily. Most patients with a microvascular abducens nerve palsy are simply observed and usually recover within 3-6 months. Treatment for the diplopia associated with abducens nerve palsy can be managed with prisms, occlusion, botulinum toxin, or surgery.[16] Occlusion using a Bangerter filter or patch can eliminate diplopia and confusion, prevent amblyopia or suppression in children, and decrease the possibility of ipsilateral medial rectus contracture. Base-out Fresnel or ground-in prisms can be used to help the patient maintain binocular single vision in the primary position, but are not usually useful due to the incomitance of the deviation. Botulinum toxin injections into the medial rectus of the affected eye are sometimes used to prevent secondary contracture of the medial rectus, or during transposition procedures to weaken the non-operative muscle. In general, surgical intervention is reserved for patients who have had stable orthoptic measurements for at least 6 months.


Strabismus surgery can be performed for persistent abducens nerve palsies that demonstrate stable measurements over a 6-month period.[14] Forced duction test is performed in the office or in the operating room in order to assist with surgical planning.

  • If there is residual lateral rectus muscle function: often, a resection of the affected lateral rectus and recession of the ipsilateral medial rectus (recess/resect or “R and R” procedure) is performed. Alternatively, a resection of the affected lateral rectus with a recession of the contralateral medial rectus may be performed.
  • Diagram of superior rectus transposition for the treatment of abducens nerve palsy. Abbreviations: SR: Superior rectus, IR: Inferior rectus LR: Lateral rectus SO: Superior Oblique
    If there is no lateral rectus muscle function: various forms of transposition surgeries can be considered (e.g., full tendon transposition, Jensen, Hummelsheim, Augmented Hummelsheim with resections +/- Foster modifications, Modified Nishida). Superior rectus transposition combined with medial rectus recession has been shown to improve esotropia, head position, and abduction in patients with abducens palsy.[21]
  • Botulinum toxin injections to the medial rectus of the affected eye can also be used as a temporizing treatment.

Surgical follow up

Patients may be managed closely postoperatively, and any residual diplopia can be managed with prisms.


The most likely complication following surgical correction of abducens nerve palsy is the risk of over- or under-correction, which may be managed postoperatively with prisms.


The prognosis for abducens nerve palsy depends on the underlying etiology. One study reported a recovery rate of 49.6% in 419 non-selected sixth nerve palsy cases, and a higher rate of 71% in 419 patients with diabetes mellitus, hypertension, or atherosclerosis.[22]


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