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A random Abstract
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Chromosomal structural analysis in carcinoma of the gallbladder.
[carcinoma of the gallbladder]
The
etiopathogenesis
of
gallbladder
cancer
is
still
unknown
.
Both
environmental
and
patient
factors
have
been
incriminated
in
its
cause
.
That
it
is
found
in
pockets
of
epidemiological
distribution
raises
an
issue
of
genetic
changes
associated
with
it
.
The
aim
of
this
study
was
to
find
out
the
chromosomal
changes
in
gallbladder
cancer
.
Lymphocyte
cell
culture
was
carried
out
on
blood
of
gallbladder
cancer
patients
to
determine
chromosomal
banding
abnormalities
.
Native
PAGE
was
also
evaluated
to
analyze
lactate
dehydrogenase
(
LDH
)
,
superoxide
dismutase
(
SOD
)
and
catalase
enzyme
activity
from
the
same
blood
of
gallbladder
cancer
patients
.
Out
of
30
gallbladder
cancer
patients
,
4
male
showed
breakage
on
the
long
arm
of
chromosome
1
while
only
one
male
patient
showed
the
translocation
from
the
long
arm
of
chromosome
4
to
the
long
arm
of
chromosome
6
in
a
male
patient
.
The
aberrations
found
in
our
study
may
suggest
underlying
genetic
predisposition
for
the
development
of
gallbladder
cancer
.
They
can
act
as
a
marker
for
gallbladder
cancer
,
which
needs
further
study
.
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