7. Clinical evaluation
2. Measurement
2. Palpebral fissure height (normal 7-10 in male,
8-12 in female).
Normal UL cover 2mm of sup limbus & 1mm of inf
limbus.
Mild: 2mm
Moderate: 3mm
Severe: > 4mm with other eye
10. Ptosis
Congenital Senile
Age (+ old photo) Since birth old
Laterality Uni/ bi bi
Severity Severe Mild
UL crease Absent Preserved
On downgaze Lid lag Ptosis is worse
LFT Poor Good
Associated signs SR weakness, MG winking,
BPS
Lax lid, deep sulcus
TTT Brow suspension Aponeurotic repair
12. Clinical evaluation
3. Associated signs
• Horner, 3rd n palsyPupil
• Manual elevate the ptotic lid, the other retracted lid will
drop (warn pt for post op other lid ptosis.Increase innervation
• In congenital, SR -- , surgical repair of hypotropia before lid
• In paralytic, 3rd n palsy, multiple n palsies, aberrant
regerneration
Ocular motility defect
• MGJW
• Ask to chew, move jaw from side to side --- improved
ptosis.
Jaw winking
• AD, Epicathus inversus, telecanthusBlepharophimosis S
• Post op assessment
• Ask pt to close lid and manually evaluate globe elevation
Bell phenomenon
• With MG
• Ask to look upward for 30 sec --- progressive lid drop.
Cogan lid twich during saccade from downgaze to PP
Fatigablity
13. Clinical evaluation
3. Associated signs
• MGJW, blepharophimosis, SR (surgery!), DEP,
CFEOM -ve Bell phenomenon, other eye!!
• Absent crease, poor LFT.
Congenital ptosis
• EOM, pupilParalytic
• Fatigability, variable, diplopiaMG
• High crease, good LFT, bil, muller
fatigue variability (milder than MG!!)Involutional
CFEOM (congenital fibrosis of EOM), DEP
(Double Elevator Palsy)
24. Central, steady maintained (CMS) fixation. Fix & follow
If squint (fixated eye/ refixation of covered eye?)
No squint --- 10 D prism base down
Vision
Pupil
Pupil
Dimlight
Horner
Bright light
3rd n palsy
Anisocoria
25. AHP, chin up (amblyopia?)
Measurement (LFT, MRD, PFH, Crease hight)
Bell phenomenon, MGJW
EOM (3rd n, DEP, Cngenital fibrosis $)
No squint --- 10 D prism base down
SLE (hypochromia ant, post segment), cyclo refraction
Exam.
26. • Rt UL congenital ptosis
with chin up.
• Chin up → No amblyopia.
30. 66 y old , ↑droppy lid over 20y,
upgaze view in photo.
BCVA 6/18 ou, EOM↓ even
with Doll̛s, -ve FDT, absent
Bell̛s.
DD:
CPEO
MG
MD
dorsal midbrain lesion
vertical gaze palsy
TED
59. Congenital lid anomalies
Lid eversion
Ecthyosis, down
Bilateral, symmetrical
May resolve spontanously
Ablepharon
No lid
60. Lid lesions (benign, malignant) √
(look at lid lesion previous ppt)
Lid malposition (ptosis, entropion, ectropion) √
Inflamation (allergic, bacterial, viral, anterior, posterior, angular
blepharitis, childhood blepharoconjunctivitis) √
Congenital (entropion, epiblepharon, telecanthus, epicanthus
fold, blepharophimosis, coloboma, cryptophthalmos,
eublepharon, ablepharon, ankyloblepharon, lid eversion) √
Miscellaneous (floppy lid, blepharochalasis,
dermatochalasis, eye imbrication, lid retraction, varices,
trichomegaly, lash ptosis, madarosis, poliosis, distichiasis)
61. Floppy lid syndrome
Floppy eye lid $
Obese middle age male,
snoring, SAS
Lid over pillow… OSD
Rubbery tarsus, papillary
conjunctivitis, PEK
TTT
Mild – taping,
lubricants
Severe – pentagon
excision
62. Blepharochalasis
Blepharochalasis
Bil recurrent episodes of ,
lid non-pitting odema,
resolving after few days.
Atrophies,wrinked skin,
LCT & LPA dehescience, fat
prolapse.
TTT
Redundant skin
blepharoplasty.
Aponeurotic ptosis
repair.