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Cowden syndrome: Recognizing and managing a not-so-rare hereditary cancer syndrome.
[cowden syndrome]
Cowden
syndrome
(
CS
)
is
an
autosomal
dominant
hereditary
cancer
syndrome
causing
increased
risk
for
breast
,
thyroid
,
renal
,
uterine
,
and
other
cancers
as
well
as
benign
neoplasias
and
neurodevelopmental
concerns
.
Timely
diagnosis
of
affected
patients
is
key
,
as
early
recognition
allows
for
high
-risk
screening
and
other
preventative
measures
prior
to
a
patient
enduring
multiple
cancer
diagnoses
.
This
review
will
highlight
the
cardinal
features
of
CS
and
management
recommendations
for
affected
patients
.
J
.
Surg
.
Oncol
.
©
2014
Wiley
Periodicals
,
Inc
.
Diseases
Validation
Diseases presenting
"early recognition"
symptom
22q11.2 deletion syndrome
cadasil
child syndrome
cowden syndrome
cushing syndrome
cystinuria
familial mediterranean fever
homocystinuria without methylmalonic aciduria
kindler syndrome
legionellosis
oligodontia
omenn syndrome
pyomyositis
thoracic outlet syndrome
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