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A random Abstract
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The Cohen syndrome: report of a case.
[cohen syndrome]
We
report
on
a
sporadic
case
satisfied
with
a
proposed
diagnostic
criteria
for
Cohen
syndrome
.
This
10
year
-old
Japanese
boy
had
truncal
obesity
,
short
stature
,
mild
mental
retardation
,
hypotonia
,
maxillary
hypoplasia
,
micrognathia
,
narrow
hands
and
feet
,
high-arched
palate
,
prominent
upper
central
incisors
,
high
nasal
bridge
,
but
no
pigmentary
retinopathy
.
Autosomal
recessive
manner
of
inheritance
was
suggested
by
the
pedigree
.
Diseases
Validation
Diseases presenting
"maxillary hypoplasia"
symptom
cohen syndrome
oligodontia
This symptom has already been validated