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The ophthalmic findings in Cohen syndrome.
[cohen syndrome]
Cohen
syndrome
is
an
uncommon
autosomal
recessive
condition
comprising
a
characteristic
facial
appearance
,
mental
retardation
,
benign
neutropenia
,
and
retinal
dystrophy
.
This
study
aimed
to
identify
patients
with
Cohen
syndrome
from
across
the
United
Kingdom
in
order
to
define
the
variability
of
ophthalmic
manifestations
.
Ophthalmic
assessment
was
undertaken
and
past
ophthalmic
records
reviewed
in
22
patients
with
classic
features
of
Cohen
syndrome
.
All
patients
had
visual
problems
which
commonly
started
in
the
preschool
years
.
82
%
developed
strabismus
or
refractive
error
during
the
first
5
years
of
life
.
70
%
developed
high
myopia
by
the
second
decade
.
By
contrast
with
the
findings
of
others
,
early
onset
retinal
dystrophy
was
common
,
occurring
in
80
%
of
study
patients
under
age
5
years
.
35
%
of
patients
were
registered
partially
sighted
or
blind
.
The
ophthalmic
abnormalities
associated
with
Cohen
syndrome
,
including
high
myopia
and
a
generalised
,
severe
retinal
dystrophy
,
are
of
early
onset
and
frequently
result
in
severe
visual
handicap
.
Cohen
syndrome
should
be
considered
in
the
young
,
developmentally
delayed
child
who
presents
with
severe
myopia
and
nyctalopia
.
Diseases
Validation
Diseases presenting
"early onset"
symptom
22q11.2 deletion syndrome
alexander disease
alpha-thalassemia
benign recurrent intrahepatic cholestasis
cadasil
canavan disease
coats disease
cohen syndrome
congenital diaphragmatic hernia
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erythropoietic protoporphyria
fabry disease
familial mediterranean fever
homocystinuria without methylmalonic aciduria
inclusion body myositis
kindler syndrome
krabbe disease
papillon-lefèvre syndrome
primary hyperoxaluria type 1
pyruvate dehydrogenase deficiency
scrub typhus
sneddon syndrome
triple a syndrome
von hippel-lindau disease
werner syndrome
wolf-hirschhorn syndrome
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