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Cowden syndrome-a case report emphasizing the role of the dental surgeon in diagnosis.
[cowden syndrome]
Cowden
syndrome
or
multiple
hamartoma
syndrome
,
is
a
rare
genetic
condition
inherited
in
an
autosomal
dominant
pattern
characterized
by
cutaneous
manifestations
,
polyps
,
thyroid
gland
neoplasias
,
and
macrocephaly
.
This
report
presents
the
case
of
a
36
-
year
-old
patient
who
looked
for
dental
treatment
for
a
gingival
nodule
.
Current
and
past
medical
history
and
oral
and
facial
manifestations
led
to
the
diagnosis
of
Cowden
syndrome
.
This
case
report
emphasizes
the
role
of
the
dental
surgeon
in
the
diagnosis
of
this
systemic
disease
,
based
on
the
analysis
of
medical
history
and
manifestations
in
the
oral
cavity
.
Diseases
Validation
Diseases presenting
"rare genetic condition"
symptom
congenital toxoplasmosis
cowden syndrome
epidermolysis bullosa simplex
homocystinuria without methylmalonic aciduria
kabuki syndrome
oculocutaneous albinism
phenylketonuria
wolf-hirschhorn syndrome
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