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Lidptosis

Lidptosis, commonly referred to as ptosis or blepharoptosis, is the drooping of the upper eyelid. It can involve one eye (unilateral) or both (bilateral) and may be present at birth or develop later in life. Ptosis results from dysfunction of the eyelid elevator muscles (primarily the levator palpebrae superioris and its aponeurosis) or from impaired nerve supply, muscle disease, mechanical weight, or eyelid elevation strategies.

Ptosis is typically classified as congenital or acquired. Congenital ptosis arises from developmental abnormalities of the

Assessment relies on objective measurements. Clinicians record the margin reflex distance 1 (MRD1), eyelid crease height,

Treatment is tailored to cause and functional impact. Asymptomatic ptosis without visual compromise may be observed.

Epidemiology varies by cause; age-related aponeurotic ptosis is common in older adults, while congenital ptosis is

levator
muscle
or
its
innervation
and
often
presents
with
reduced
eyelid
lift
and
limited
levator
function.
Acquired
ptosis
has
several
subtypes:
aponeurotic
(age-related
detachment
of
the
levator
aponeurosis,
common
in
older
adults);
neurogenic
(due
to
oculomotor
nerve
palsy
or
Horner
syndrome);
myogenic
(muscle
diseases
such
as
muscular
dystrophy
or
myasthenia
gravis);
mechanical
(lid
heaviness
from
swelling
or
lesions);
and
traumatic
or
iatrogenic
causes.
and
levator
function
(degree
of
eyelid
movement
from
downgaze
to
upgaze).
The
examination
may
include
assessment
for
anisocoria,
pupil
involvement,
and
signs
of
neuromuscular
or
autonomic
disease.
Laboratory
tests,
imaging,
and
specific
tests
(eg,
ice
test
or
edrophonium
test
for
myasthenia
gravis)
may
be
used
to
identify
underlying
causes.
Congenital
ptosis
with
poor
vision
risk
often
requires
surgical
correction,
typically
levator
resection/advancement
or
frontalis
suspension.
Acquired
ptosis
treatment
targets
the
underlying
condition
and
may
involve
similar
eyelid
surgery
if
visual
field
loss
persists.
Outcomes
depend
on
etiology,
levator
function,
and
patient-specific
factors.
relatively
rare.
See
also
blepharoptosis
and
eyelid
disorders.