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Genetic/familial high-risk assessment: breast and ovarian, version 1.2014.
[cowden syndrome]
During
the
past
few
years
,
several
genetic
aberrations
that
may
contribute
to
increased
risks
for
development
of
breast
and
/
or
ovarian
cancers
have
been
identified
.
The
NCCN
Guidelines
for
Genetic
/
Familial
High
-
Risk
Assessment
:
Breast
and
Ovarian
focus
specifically
on
the
assessment
of
genetic
mutations
in
BRCA
1
/
BRCA
2
,
TP
53
,
and
PTEN
,
and
recommend
approaches
to
genetic
testing
/
counseling
and
management
strategies
in
individuals
with
these
mutations
.
This
portion
of
the
NCCN
Guidelines
includes
recommendations
regarding
diagnostic
criteria
and
management
of
patients
with
Cowden
Syndrome
/
PTEN
hamartoma
tumor
syndrome
.
Diseases
Validation
Diseases presenting
"several genetic aberrations that may contribute to increased risks for development of breast and"
symptom
cowden syndrome
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