Rare Diseases Symptoms Automatic Extraction
Home
A random Abstract
Our Project
Our Team
Unilateral optic atrophy preceding Coats disease in a girl with Parry-Romberg syndrome.
[coats disease]
Parry-
Romberg
syndrome
(
PRS
)
is
a
rare
disease
of
unknown
etiology
and
pathogenesis
,
characterized
by
progressive
hemifacial
atrophy
.
Diverse
ocular
manifestations
were
reported
in
association
with
PRS
,
including
enophthalmos
,
lid
retraction
,
blepharoptosis
,
restrictive
strabismus
,
ocular
motor
nerve
dysfunction
,
Horner
syndrome
,
reduced
corneal
sensitivity
,
band
keratopathy
,
episcleritis
,
uveitis
,
neuroretinitis
,
and
retinal
vasculitis
.
Descriptive
case
report
.
We
report
on
the
development
of
unilateral
optic
atrophy
followed
by
ipsilateral
Coats
disease
exudation
and
shallow
retinal
detachment
in
the
posterior
pole
and
inferior
retina
.
Optic
atrophy
was
not
previously
described
in
association
with
PRS
.
We
describe
the
development
of
unilateral
optic
atrophy
with
subsequent
CD
,
5
years
later
,
in
a
girl
with
PRS
.
Diseases
Validation
Diseases presenting
"hemifacial atrophy"
symptom
coats disease
This symptom has already been validated