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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
"developmentally delayed child"
symptom
cohen syndrome
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