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A random Abstract
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Hereditary gynaecological malignancies: advances in screening and treatment.
[cowden syndrome]
In
the
last
two
decades
there
have
been
significant
advances
in
our
understanding
of
female
genital
tract
tumours
.
The
discovery
of
BRCA
1
and
BRCA
2
genes
in
ovarian
cancer
and
the
mismatch
repair
genes
in
endometrial
carcinoma
has
revolutionized
our
approach
to
the
diagnosis
and
screening
of
women
for
ovarian
and
uterine
cancers
.
This
review
discusses
the
pathogenesis
of
these
two
hereditary
syndromes
in
depth
and
explains
how
the
molecular
genetics
is
tailoring
the
manner
in
which
these
diseases
are
diagnosed
and
potentially
treated
.
Other
,
less
common
hereditary
conditions
associated
with
gynaecological
tract
manifestations
,
such
as
Cowden
syndrome
,
Peutz-
Jeghers
syndrome
,
Gorlin
syndrome
and
hereditary
leiomyomatosis
and
renal
cell
carcinoma
,
are
also
summarized
briefly
.
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