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Ptosis and Lid Lag

Ptosis is a term applied to drooping of the eyelid. It can be unilateral or bilateral, complete or incomplete, acquired or congenital. Lid lag means delay in moving the eye lid as the eye moves downwards. It is a common finding in thyroid disease, when it is known as von Graefe's sign.1

Epidemiology

There is no race or gender predilection. Acquired ptosis can occur at any age.2 Congenital ptosis usually presents at birth but is sometimes detected within the first year of life.3

Presentation

Ptosis

History

Adults usually notice a change in their appearance, and may complain that they always look sleepy and tired.2 They may also note reduced visual fields. A history should cover the date of onset, any previous trauma or eye surgery, relieving or aggravating surgery, and any relevant family or medical history. In children with congenital ptosis, there is a history of unilateral or bilateral drooping eyelid, the onset of which may be elicited by looking at family photographs if available.3 On examining such photographs, other relatives with ptosis may be identified, in which case a familial cause is highly likely.
The history should also enquire about:

  • Medication and allergy reactions - eyelid oedema can mimic ptosis
  • Fluctuating ptosis - may indicate myasthenia gravis
  • History of cancer or symptoms indicative of cancer - metastases or primary orbital tumours can cause malposition of the eyelid
  • A history of trauma - a fractured orbit can result in pseudoptosis with enophthalmos. A third nerve palsy may also result in ptosis.

Examination

A limited examination can be conducted in primary care, but various measurements can be taken, including:

  • The palpebral fissure (PF) - the distance between the upper and lower eyelid in vertical alignment with the centre of the pupil
  • The marginal reflex distance-1 (MRD-1) - the distance between the centre of the pupillary light reflex and the upper eyelid margin with the eye in primary gaze
  • MRD-2 - the distance between the center of the pupillary light reflex and the lower eyelid margin with the eye in primary gaze
  • Levator function - the distance the eyelid travel from downgaze to upgaze while the frontalis muscle is held inactive at the brow
  • The margin fold distance (MFD) - the distance from the upper eyelid margin to the fold of skin.

Other features to look out for on examination include:

  • Abnormalities of tear production
  • Lower eyelid laxity or scleral show
  • Lagophthalmos (difficulty in complete closure of the eyelid over the eyeball)
  • Anterior displacement of the globe within the orbit
  • Pseudoptosis can result from a number of conditions that alter the appearance of the eyeball (see Differential Diagnosis, below)
  • Eyelid retraction requires exclusion of thyroid orbitopathy.

Lid lag

This is not normally noticed by the patient, but is discovered when a patient with thyroid disease has an eye examination. The feature is elicited by asking the patient to follow with their eyes an object moving slowly from their upper to lower field of vision, and vice versa. In lid lag, the upper eyelid lags behind the upper edge of the iris as the eye moves downward. A similar phenomenon is seen with the lower edge, when the eye moves upwards. If the object is moved too quickly, the diagnosis may be missed.

Differential diagnosis

Differential Diagnosis of Congenital Ptosis

Chronic Progressive External
Ophthalmoplegia (a disorder characterized by slowly progressive paralysis of the extraocular muscles)
Myasthenia Gravis Papilloedema
Acquired myogenic ptosis Aponeurotic ptosis (the result of a failure of the distal end of the aponeurosis to attach in the usual position) Neurogenic ptosis
Mechanical ptosis Traumatic ptosis Pseudoptosis - usually caused by alteration in the appearance of the orbit such as microphthalmos, enophthalmos or orbital fracture
Blepharochalasis (relaxation of the skin of the eyelid, due to atrophy of the intercellular tissue) Myotonic dystrophy Kearns-Sayre syndrome - this triad includes onset in persons younger than 20 years, chronic, progressive, external ophthalmoplegia and pigmentary degeneration of the retina
                                            Acquired Blepharoptosis (see Adult Ptosis)

There is a long list of conditions which enter the differential diagnosis of acquired ptosis. The main ones are as follows:2

Differential Diagnosis of Acquired Ptosis

Anophthalmos Bell Palsy Blepharospasm, Benign Essential
Cellulitis, Orbital Cellulitis, Preseptal Chalazion
Chronic Progressive External Ophthalmoplegia Conjunctivitis, Giant Papillary Corneal Abrasion
Corneal Foreign Body Dermatitis, Atopic Duane Syndrome (dysfunction of the eye muscles,
normally evident by the age of ten)
Exophthalmos Haemangioma, Capillary Horner Syndrome
Laceration, Eyelid Lyme Disease Marcus Gunn Jaw-winking Syndrome
Multiple Sclerosis Myasthenia Gravis Neuro-ophthalmic History
Neurofibromatosis-1 Oculomotor Nerve Palsy Orbital Fracture, Apex
Orbital Fracture, Floor Ptosis, Congenital Thyroid Ophthalmopathy
Investigations

Congenital ptosis3

Test to exclude myasthenia gravis such as serum acetylcholine receptor antibody level, edrophonium chloride (Tensilon) test and EMG should be checked if this condition is suspected.
MRI or CT of orbit and brain may helpful in certain circumstances, e.g.:

  • The diagnosis is not evident from the history and examination
  • A history of trauma suggests orbital fracture
  • Other neurological symptoms are suggestive of neurological disease
  • There is a visible or palpable lid mass
  • There is a suspicion of orbital tumours
  • There is new onset Horner syndrome or third cranial nerve palsy, with or without other neurological findings
  • Enophthlamos or proptosis is present with globe displacement.

Other investigations

Depending on the presentation, other relevant tests may be needed such as mitochondrial assays to exclude mitochondrial disorders of the muscle.

Adult ptosis

  • Tests for myasthenia gravis as above
  • ECG, EMG, mitochondrial studies and electroretinogram may be needed to exclude chronic progressive external ophthalmoplegia
  • Consider thyroid function tests for patients with suspected thyroid ophthalmopathy.

Lid lag4

Thyroid function tests should be performed. CT scan of the orbit may be required in cases of diagnostic difficulty.

Associated diseases

Congenital ptosis

This is often idiopathic but may be associated with:

  • Poor visual acuity or strabismus
  • Birth trauma
  • Peri-orbital tumours
  • Neuroma or neurofibroma
  • Neuropathic:
    • Horner's syndrome
    • 3rd nerve lesion
    • Marcus Gunn jaw-winking syndrome - eye winks when jaw moves, also known as trigemino-oculomotor synkinesis, thought to be an aberrant connection between the motor branches of the trigeminal nerve and fibres of the superior division of the oculomotor nerve.5

Acquired

  • Horner's syndrome - paralysis of the sympathetic nerves, causing unilateral ptosis with ipsilateral constriction of the pupil, and sweating
  • 3rd nerve lesion - usually complete ptosis, with ophthalmoplegia with a dilated, unreactive pupil
  • Plexiform neuroma - this is associated with neurofibroma type 1
  • Myopathy - e.g. myasthenia gravis - the ptosis may be unilateral or bilateral
  • Levator dehiscence (aponeurotic ptosis) - this is due to a dysfunction of the superior rectus-levator muscle. It may be iatrogenic (e.g. damage during suturing) in which case the condition is unilateral, or degenerative due to senility, which is usually bilateral.

Lid lag

The majority of lid lag is seen in thyroid ophthalmopathy (also known as Graves' ophthalmopathy). In one study of 120 patient with thyroid ophthalmopathy, 43% had lid lag.6 Other common associated conditions are Graves' disease in children, hyperthyrotoxicosis and anxiety (all these are reflections of increased adrenergic tone).

Management

Congenital ptosis3

  • Mild cases may require no initial treatment. The patient should however be monitored every 3-4 months for signs which suggest the development of amblyopia (poor or blurry vision, usually in one eye, also called 'lazy eye'), strabismus, or abnormal head posture.
  • Surgical treatment should be considered for patients who start to develop complications. The type of operation depends on the underlying diagnosis and the degree of function of the levator muscle. Options include levator muscle suspension, suspension of the frontalis muscle (tightening of the brow muscles), and rarely in congenital cases, the Fansella-Servat procedure in which a block of tissue is removed from the underside of the lid.

Adult ptosis2

  • Underlying disease should be treated (e.g. myasthenia gravis)
  • Patients who do not wish to undergo surgery may prefer tape the lid using micropore tape. They should also used lubricants when employing this method, as the blinking mechanism will be less efficient. Alternatively, some patients may wish to use spectacles with a lid attachment which holds up the eyelid.
  • Surgical options include frontalis slings, levator resection, correction of any abnormality of the levator muscle, and the Fansella-Servat procedure.

Lid lag

This causes no subjective symptoms and therefore does not require treatment, but may resolve when the patient becomes euthyroid.

Complications

Congenital ptosis

Complications may include amblyopia, strabismus and abnormal posture of the head (the chin-up position).

Adult ptosis

Reduced field of vision and headaches due to tension of the frontalis muscle can occur. Anxiety about appearance may result in social isolation and cause significant psychological complications.

Lid lag

There are no significant complications.

Prognosis

Congenital ptosis3

Surgical correction usually produces excellent results, and amblyopia can be treated successfully if detected early enough.

Adult ptosis

  • The treatment of myasthenia gravis results in the correction of ptosis in about 70% of patients7
  • Excellent results are usually achieved when operative procedures are performed by experienced surgeons.8

Document references
  1. Friedrich Wilhelm Ernst Albrecht von Graefe (www.whonamedit.com).
  2. Cohen A; Emedicine Ptosis Adult 2006
  3. Suh D; Congenital Ptosis. eMedicine, November 2007.
  4. GP Notebook; Lid Lag
  5. Blaydon S 2006; Marcus Gunn Jaw-winking Syndrome
  6. Bartley GB, Fatourechi V, Kadrmas EF, et al; Clinical features of Graves' ophthalmopathy in an incidence cohort.; Am J Ophthalmol. 1996 Mar;121(3):284-90. [abstract]
  7. Kupersmith MJ, Ying G; Ocular motor dysfunction and ptosis in ocular myasthenia gravis: effects of treatment.; Br J Ophthalmol. 2005 Oct;89(10):1330-4. [abstract]
  8. Bashour M, Blepharoplasty, Ptosis Surgery eMedicine
Acknowledgements EMIS is grateful to Dr Laurence Knott for writing this article. The final copy has passed scrutiny by the independent Mentor GP reviewing team. ©EMIS 2008.
DocID: 1600
Document Version: 22
DocRef: bgp112
Last Updated: 25 Sep 2006
Review Date: 24 Sep 2008
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