Rare Diseases Symptoms Automatic Extraction
Home
A random Abstract
Our Project
Our Team
Ocular manifestations in Wolf-Hirschhorn syndrome.
[wolf-hirschhorn syndrome]
Wolf-
Hirschhorn
syndrome
(
WHS
)
multiple
congenital
anomalies
/
mental
retardation
is
caused
by
partial
deletion
of
the
short
arm
of
chromosome
4
and
can
be
considered
a
contiguous
gene
syndrome
,
characterized
by
typical
facial
appearance
,
mental
retardation
,
growth
delay
,
and
seizures
.
We
investigated
the
ocular
defects
in
a
population
of
10
patients
with
WHS
and
analyzed
the
relationship
between
ocular
findings
and
the
extent
of
deletion
on
chromosome
4
.
T
he
ocular
abnormalities
found
included
hypertelorism
,
strabismus
,
refractive
errors
,
epicanthal
folds
,
proptosis
,
downslanting
palpebral
fissures
,
microphthalmos
,
microcornea
,
iris
coloboma
,
optic
nerve
coloboma
,
ocular
cyst
,
ptosis
,
glaucoma
,
and
nystagmus
.
Different
breakpoints
of
the
chromosomal
rearrangement
were
observed
in
individual
patients
,
ranging
from
4
p
15
.
1
to
4
p
16
.
3
,
and
the
size
of
chromosomal
deletion
ranged
from
2
.
6
to
26
million
base
pairs
.
Congenital
glaucoma
and
colobomatous
ocular
cysts
have
rarely
been
described
in
WHS
patients
that
were
previously
reported
.
In
all
cases
exhibiting
strabismus
,
an
exodeviation
was
present
.
Comparing
genotype
with
ocular
phenotype
,
a
relationship
between
the
size
of
deletion
and
the
severity
of
the
ocular
involvement
was
observed
in
all
cases
but
one
.
Diseases
Validation
Diseases presenting
"mental retardation"
symptom
achondroplasia
alexander disease
alpha-thalassemia
aniridia
aromatase deficiency
canavan disease
classical phenylketonuria
coats disease
cohen syndrome
cowden syndrome
cystinuria
dentin dysplasia
familial hypocalciuric hypercalcemia
homocystinuria without methylmalonic aciduria
hydrocephalus with stenosis of the aqueduct of sylvius
kabuki syndrome
kallmann syndrome
lamellar ichthyosis
lymphangioleiomyomatosis
monosomy 21
phenylketonuria
primary hyperoxaluria type 1
proteus syndrome
pyruvate dehydrogenase deficiency
sneddon syndrome
triple a syndrome
wolf-hirschhorn syndrome
zellweger syndrome
This symptom has already been validated