Congenital ptosis is caused by weakness of the levator palpebrae superioris muscle. It is characterized by drooping of one or both eyelids, especially since birth. The ptotic eyelid is higher than normal on downgaze due to tethering of the abnormal LPS muscle. Congenital ptosis can be associated with blepharophimosis syndrome or Marcus Gunn jaw-winking syndrome. Treatment depends on severity, ranging from tarsal conjunctival resection for mild ptosis to frontalis brow suspension for severe ptosis with no levator function.

2. Ptosis ( in greek means to fall) is the
abnormal drooping of the upper eyelid.
Normally upper lid covers about upper
one sixth of the cornea i.e about 2mm.
Therefore in ptosis it covers more than
2 mm.

3. Congenital
Acquired
Pseudotosis
Neurogenic
Myogenic
Aponeurotic
Mechanical
Neurotoxic

4. ETIOLOGY:
It is associated with congenital weakness of the LPS.
CHARACTERISTIC FEATURES:
- Drooping of one or both upper lids more often since
birth of variable severity ( mild,moderate or severe).
- Lid lag on downgaze( i.e. ptotic lid is higher than the
normal) due to tethering effect of abnormal LPS
muscle. This is in contrast to acquired ptosis in which
ptotic lid is lower than the normal in downgaze also.
- LPS function may be poor, fair or good depending upon the
degree of weakness.

5. ASSOCIATED
FEATURES
Simple congenital
ptosis
Congenital
ptosis
Blepharophimosis
Congenital
synkinetic
ptosis

6. 1.) SIMPLE CONGENITAL
PTOSIS:
- Not associated with any
other anomaly.
2.) CONGENITAL PTOSIS:
- Associated with weakness of superior rectus
muscle.

7. 3.) BLEPHAROPHIMOSIS SYNDROME:
- Rare congenital disorder.
- Short horizontal palpebral aperture.
- Telecanthus:
Lateral displacement of medial
canthus.
- Epicanthus inversus:
Lower lid fold larger than upper lid.
- Lateral inferior ectropion.
- Poorly developed nasal bridge and
hypoplasia of superior orbital rims.

9. 4.) CONGENITAL SYNKINETIC PTOSIS ( MARCUS
GUNN JAW-WINKING PTOSIS):
- This condition is characterized as a synkinesis:
when two or more muscles that are
independently innervated have either
simultaneous or coordinated movements.
IN MARCUS GUNN PHENOMENON:
- The stimulation of the trigeminal nerve by
contraction of the pterygoid muscles of
jaw results in the excitation of the branch
of the oculomotor nerve that innervates
the LPS ipsilaterally, so the patient will have
rhythmic upward jerking of their upper
eyelid.

10. MARCUS GUNN JAW-WINKING SYNDROME:
- Accounts for about 5% of all cases of
congenital ptosis.
- Retraction or wink of ptotic lid in
conjunction with stimulation of ipsilateral
pterygoid muscles.

11. - Congenital or acquired .
- Eyeball is turned down, out slightly intorted due to actions
of lateral rectus and superior oblique muscles.
- ocular movements restricted in all directions except
outward.
- pupil is fixed and dilated due to paralysis of spinchter
pupillae muscle.
- accommodation is completely lost due to paralysis of ciliary
muscle.
1. NEUROGENIC PTOSIS
ETIOLOGY:
A) THIRD NERVE PALSY

12. - Rare, unilateral
- Pupil is occasionally involved
- Bizarre movements of upper lid accompany eye
movements
B) THIRD NERVE MISDIRECTION:

13. - Used to describe any oculosympathetic paresis,
wherever the lesion may be.
- Characterized by classic triad of:
Mild ptosis ( due to paralysis of muller’s muscle)
Miosis ( due to paralysis of dilator puppillae)
Reduced ipsilateral sweating ( anhydrosis)
- Other features include mild enophthalmos, loss of
cilio- spinal reflex ,heterochromia, i.e., ipsilateral
iris is lighter in colour, pupil is slow to dilate, and
there occurs slight elevation of the lower eyelid.
C) HORNER SYNDROME:

14. - rare eye disorder, previously called a
“complicated migraine” which is also
recognized as cranial neuralgia by the
internal classification of Headache
Disorders (HIS II).
- most commonly presents itself in early
childhood or infancy.
- To date there is no conclusive hypothesis as
to the etiology of this disorder.
D) OPTHALMOPLEGIC MIGRAINE:

15. - Characterized by:
~ Severe headaches
~ Weakening of muscles around the eye.
~ These headache commonly precede
episodes of partial paralysis of one or more
ocular nerve ( most commonly the third
cranial nerve).
~ Drooping of eyelid
~ Double vision
~ Dilation of pupils

16. - Due to supranuclear lesions.
- Unilateral cerebral ptosis occurs with lesions ,
usually ischemic, of the opposite
hemisphere, and is more common with right
hemisphere lesions.
- Bilateral supranuclear ptosis may occur with
unilateral or bilateral hemispheric lesions.
- Ptosis has been reported in as many as
37.5% of patients with hemispheric strokes.
E) CEREBRAL PTOSIS:

17. 2) MYOGENIC PTOSIS:
- It is due to acquired disorders of the LPS muscle
or of the myoneural junction.
- It may be seen in patient having:
A) MYASTHENIA GRAVIS:
- Ptosis is frequently assymetric and may be
unilateral, though it will tend to shift from side
to side .
- Characteristically fluctuates from moment to
moment and is worsened by prolonged
upgaze (fatiguable ptosis).

18. - COGAN’S LID TWITCH SIGN:
Characteristic of myasthenia, consists of a brief
overshoot twitch of lid retraction following sudden
return of the eyes to primary position after a
period of downgaze.

19. Edrophonium chloride inhibits acetylcholine at the
neuromuscular junction.
This results in enhanced muscle strength.
Positive result:
Elevation of
eyelids in 2-5
min post
administration
of Tensilon.
Negative
result:
No
improvement
within 3 min.
False Positive
result:
Occur in patient
with Lambert-Eaton
Myasthenic
Syndrome
Amyothrophic
Lateral Sclerosis
Localized
intracranial mass
lesion.
Side Effects due to
overactivation of
parasympathetic system:
fainting, dizziness,
involuntary defecation,
severe bradycardia, and
even cardiac arrest.
important to have
atropine if such side effect
occur.
INVESTIGATION:
(a) Edrophonium( Tensilon) Test:

21. (b) Electromyography to confirm fatique
(c) Antibodies to acetylcholine receptors
(d) CT or MRI for presence of thymoma
- Medical – anticholinesterases,
steroids and azathioprine
- Thymectomy
TREATMENT OPTIONS:

24. D) OCULOPHARYNGEAL
MUSCULAR DYSTROPHY
E) LAMBERT-EATON MYASTHENIA
SYNDROME

25. - Develops due to defects of the levator aponeurosis in
the presence of a normal functioning muscle.
- It includes:
• Very common. Asymmetric lids and redundant
lid tissue in the elderly.
• The levator aponeurosis attaches the levator
muscle to tarsal plate which forms the eyelid.
Involutional(senile)
ptosis
• Ptosis due to aponeurotic weakness associated
with blepharochalasis.
• Blepharochalasis is an inflammation of the
eyelid that is characterized by exacerbations and
remissions of eyelid edema, which results in a
stretching and subsequent atrophy of the eyelid
tissue resulting in redundant folds over the lid
margin.
Postoperative
ptosis
Posttraumatic dehiscence
or disinsertion of the
aponeurosis.
3.) APONEUROTIC PTOSIS:

27. 4.) MECHANICAL PTOSIS:
- Due to excessive weight on upper lid as seen in
patients with:
Lid tumours
Multiple Chalazia
Lid oedema
- Also occur due to scarring (Cicatricial ptosis) as
seen in patient with:
Ocular pemphigoid
Trachoma

28. Envenomation by elapids such as cobras or kraits.
- Bilateral ptosis is usually accompanied by
diplopia, dysphagia and progressive muscular
paralysis.
- Regardless, neurotoxic ptosis is a precursor to
respiratory failure and eventual suffocation
caused by complete paralysis of the thoracic
diaphragm.
- It is therefore a
medical emergency
and immediate
treatment is required.
5.) NEUROTOXIC PTOSIS:

29. Pseudotosis is the appearance of ptosis in the absence of
levator abnormality.
Exclude pseudoptosis ( stimulated ptosis) on inspection.
Its common causes are:
Microphthalmos
Anopthalmos
Enopthalmos
Phthisis bulbi
Double elevator palsy
Blepharospasm
Contralateral proptosis

30. 1.) Ptosis:
- Age of onset
- Duration
- One/ both eye
- Diurnal variability
2.) Associated history:
- Diplopia
- Dysphagia
- Muscle weakness
3.) Vision
A.) HISTORY:

31. 4.) Association with:
- Jaw movements
- Abnormal ocular movements
- Abnormal head posture
5.) History of:
- Trauma or previous surgery
- Poisoning
- Use of steroid drops
- Any reaction with anaesthesia
- Bleeding tendency
6.) Previous photograph may prove to be of great help.
7.) Is there a family history of ptosis or of other muscle
weakness?

32. The normal upper eyelid in primary position:
- crosses the iris between the
limbus(junction of the iris and sclera) and
the pupil,
- usually 1mm to 2mm below the limbus;
- the lower lid touches or crosses slightly
above the limbus.
- normally there is no sclera
showing above the iris.
The palpebral fissures:
- are normally 9mm to 12mm from upper
B) OCULAR EXAMINATION:
1.) NORMAL POSITION OF LID:

34. Whether ptosis is:
Unilateral/ Bilateral
Complete/ Incomplete
Function of orbicularis oculi muscle
Eyelid crease is present or absent
Jaw-winking phenomenon is present or
absent
Associated weakness of any
extraocular muscle
Bell’s phenomenon is present or
absent.
2.) OBSERVE THE FOLLOWING POINTS:

35. 3.) MEASUREMENTS:
(a) MARGIN REFLEX DISTANCE:
-When light is thrown on the cornea a
reflection occurs , the distance from the
central pupillary light reflex to the upper
eyelid margin with the eye in primary gaze.
- Normal: 4-5mm
-If the margin is above the light reflex the
MRD is a +ve value.
- If the lid margin is below the corneal reflex
in cases of very severe ptosis the MRD would
be a –ve value.

37. (b) VERTICAL FISSURE HEIGHT:
- The distance between the upper and lower eyelid
in vertical alignment with the center of the pupil in
primary gaze, with the patient’s brow relaxed.
- Normal 9-10mm in primary gaze.
- Should be seen in up gaze, down gaze and
primary gaze.
- Amount of ptosis= difference in palpebral
apertures in unilateral ptosis or difference
from normal in bilateral ptosis.
GRADING OF SEVERITY OF PTOSIS:
< or =2mm : Mild ptosis
=3mm : moderate ptosis
= or > 4mm : Severe ptosis

40. - It is determined by the lid excursion caused by LPS
muscle ( Burke’s Method).
~Patient is asked to look down and thumb of one
hand is placed firmly against the eyebrow of the
patient( to block the action of frontalis muscle)
by the examiner.
~Then the patient is asked to look up and the
amount of upper lid excursion is measured with
a ruler held in the other hand by the examiner.
- Levator function is graded as follows:
Normal: 15mm
Good
Fair
Poor
: 8mm or more
: 5-7mm
: 4mm or less
( c) LEVATOR FUNCTION ASSESMENT:

42. Almost needs surgical correction. In severe
ptosis, surgery should be performed at the
earliest to prevent stimulus deprivation
amblyopia.
However in mild and moderate ptosis,
surgery should be delayed until the age of
34 years, when accurate measurements are
possible.
1.) CONGENITAL PTOSIS:

43. Tarso-
conjunctivo-
Mullerectomy(
Fasanella-
Servat
operation)
• Performed in cases
having mild
ptosis(1.5-2mm) and
good levator function.
In it upper lid is
everted and the
upper tarsal border
along with its
attached Muller’s
muscle and
conjunctiva are
resected.
Levator
Resection
• Very commonly
performed operation
for moderate and
severe grades of
ptosis. It is
contraindicated in
patients having severe
ptosis with poor
levator function.
Frontalis Brow
Suspension
• Performed in patients
having severe ptosis
with no levator
function. In this
operation, lid is
anchored to the
frontalis muscle via a
sling. Fascia lata or
some non absorbable
material ( e.g.
supramide suture,
silicon rod) may be
used as a sling.

47. - Treat the underlying cause wherever
possible.
- Conservative treatment should be carried
out and surgery deffered atleast for 6 months
in neurogenic ptosis.
- Surgical procedures ( when required) for
acquired ptosis are essentially the same as
described for congenital ptosis. However the
amount of levator resection required is always
less than the congenital ptosis of the same
degree. Further in most cases the simple
Fasanella-Servat procedure is adequate.
2.) ACQUIRED PTOSIS: