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Tissue specific somatic mutations and aganglionosis in Hirschsprung's disease.
[hirschsprung disease]
RET
proto-oncogene
intron
1
variations
[
e
.
g
.
SNP
1
(
rs
2506004
)
and
SNP
2
(
rs
2435357
)
]
have
been
shown
to
be
etiologically
important
in
the
pathogenesis
of
Hirschsprung
's
disease
(
HSCR
)
.
Although
activating
somatic
RET
rearrangements
have
been
identified
in
certain
tumours
,
this
is
the
first
study
to
confirm
somatic
gene
variation
in
HSCR
.
DNA
was
extracted
from
53
paraffin
embedded
tissue
samples
(
HSCR
patients
n
=
33
,
multiple
levels
n
=
17
)
,
and
controls
(
n
=
3
)
.
Patients
were
grouped
into
aganglionic
(
Group
1
)
,
ganglionated
(
group
2
)
,
and
transitional
(
group
3
)
.
PCR
products
of
RET
intron
1
were
screened
for
genetic
variation
by
semi-automated
bi
-directional
sequencing
analysis
and
matched
to
unaffected
controls
from
the
general
population
.
Comparison
was
by
Fishers
exact
test
.
P
<
0
.
05
was
regarded
as
significant
.
HSCR
patients
included
short
segment
(
n
=
26
)
,
long
segment
colonic
[
(
n
=
4
(
24
%
)
]
,
and
total
colonic
aganglionosis
(
n
=
3
)
.
RET
intronic
variations
[
SNP
1
(
rs
2506004
)
or
SNP
2
(
rs
2435357
)
]
showed
somatic
homozygous
in
affected
tissue
in
9
/
12
(
75
%
)
Group
1
(
aganglionic
tissue
)
compared
with
2
/
5
(
40
%
)
and
1
/
10
(
10
%
)
of
groups
2
and
3
(
P
<
0
.
001
)
.
Homozygous
SNP
2
variation
was
observed
in
all
long
segment
versus
4
/
10
short
segment
.
50
%
of
the
short
segment
cases
showing
homozygous
SNP
1
variation
.
We
report
somatic
mutations
in
the
RET
intron
1
region
of
affected
HSCR
tissue
,
confirming
for
the
first
time
that
somatic
mutations
are
present
in
aganglionic
tissue
and
may
promote
local
aganglionosis
through
deregulated
receptor
activity
.
Detailed
understanding
of
the
somatic
genetic
events
that
drive
congenital
aganglionosis
may
have
bearing
on
diagnosis
and
therapy
.
Diseases
Validation
Diseases presenting
"first time"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
adrenomyeloneuropathy
alpha-thalassemia
aniridia
aromatase deficiency
canavan disease
carcinoma of the gallbladder
cholangiocarcinoma
classical phenylketonuria
congenital adrenal hyperplasia
congenital toxoplasmosis
cowden syndrome
cushing syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dentin dysplasia
dentinogenesis imperfecta
dracunculiasis
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
fabry disease
familial mediterranean fever
gm1 gangliosidosis
harlequin ichthyosis
heparin-induced thrombocytopenia
hirschsprung disease
hodgkin lymphoma, classical
holt-oram syndrome
hydrocephalus with stenosis of the aqueduct of sylvius
junctional epidermolysis bullosa
kabuki syndrome
kallmann syndrome
liposarcoma
locked-in syndrome
lymphangioleiomyomatosis
malignant atrophic papulosis
megacystis-microcolon-intestinal hypoperistalsis syndrome
monosomy 21
neuralgic amyotrophy
oculocutaneous albinism
oligodontia
omenn syndrome
oral submucous fibrosis
papillon-lefèvre syndrome
pendred syndrome
phenylketonuria
primary effusion lymphoma
primary hyperoxaluria type 1
severe combined immunodeficiency
sneddon syndrome
triple a syndrome
trochlear dysplasia
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
zellweger syndrome
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