Rare Diseases Symptoms Automatic Extraction
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Genetic testing by cancer site: uterus.
[cowden syndrome]
This
review
article
discusses
hereditary
cancer
predisposition
syndromes
with
uterine
manifestations
.
Lynch
syndrome
accounts
for
2
%
to
3
%
of
endometrial
cancers
.
The
identification
of
endometrial
cancer
patients
at
risk
for
Lynch
syndrome
is
discussed
,
as
are
the
characteristics
of
Lynch
syndrome
-associated
endometrial
cancer
and
the
screening
and
prevention
options
for
women
at
risk
for
Lynch
syndrome
-associated
endometrial
cancer
.
Endometrial
cancer
associated
with
PTEN
hamartoma
tumor
syndrome
(
also
known
as
Cowden
syndrome
)
is
also
discussed
.
HLRCC
(
hereditary
leiomyomatosis
and
renal
cell
carcinoma
)
,
which
has
an
associated
high
risk
of
symptomatic
uterine
leiomyomas
,
is
reviewed
.
Diseases
Validation
Diseases presenting
"cancer"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
alpha-thalassemia
benign recurrent intrahepatic cholestasis
cadasil
canavan disease
carcinoma of the gallbladder
cholangiocarcinoma
coats disease
congenital adrenal hyperplasia
congenital diaphragmatic hernia
cowden syndrome
cushing syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
familial hypocalciuric hypercalcemia
familial mediterranean fever
gm1 gangliosidosis
heparin-induced thrombocytopenia
hereditary cerebral hemorrhage with amyloidosis
hirschsprung disease
hodgkin lymphoma, classical
inclusion body myositis
junctional epidermolysis bullosa
kabuki syndrome
kallmann syndrome
kindler syndrome
lamellar ichthyosis
liposarcoma
locked-in syndrome
lymphangioleiomyomatosis
monosomy 21
neuralgic amyotrophy
oculocutaneous albinism
oligodontia
oral submucous fibrosis
papillon-lefèvre syndrome
pendred syndrome
pleomorphic liposarcoma
primary effusion lymphoma
proteus syndrome
pyomyositis
pyruvate dehydrogenase deficiency
severe combined immunodeficiency
sneddon syndrome
systemic capillary leak syndrome
triple a syndrome
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
This symptom has already been validated