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Frequency of MEFV gene mutations in Hatay province, Mediterranean region of Turkey and report of a novel missense mutation (I247V).
[familial mediterranean fever]
In
the
present
study
,
1000
patients
with
clinical
suspicion
of
FMF
were
retrospectively
reviewed
to
determine
the
spectrum
of
MEFV
gene
mutations
by
using
DNA
sequence
analysis
between
September
,
2008
and
April
,
2012
.
Sixteen
different
mutations
and
55
different
genotypes
were
detected
in
618
of
1000
patients
.
Among
16
different
mutations
,
R
202
Q
(
21
.
35
%
)
was
the
most
frequently
observed
mutation
;
followed
by
E
148
Q
(
8
.
85
%
)
,
M
694
V
(
7
.
95
%
)
,
M
680
I
(
2
.
40
%
)
,
V
726
A
(
1
.
85
%
)
,
M
694
I
(
0
.
95
%
)
,
A
744
S
(
0
.
80
%
)
,
R
761
H
(
0
.
55
%
)
,
P
283
L
(
0
.
35
%
)
,
K
695
R
(
0
.
20
%
)
,
E
230
K
(
0
.
15
%
)
,
L
110
P
(
0
.
10
%
)
,
I
247
V
(
0
.
05
%
)
,
G
196
W
(
0
.
05
%
)
and
G
304
R
(
0
.
05
%
)
.
In
the
present
study
,
a
novel
missense
mutation
(
I
247
V
)
and
a
silent
variant
(
G
150
G
)
were
identified
in
the
MEFV
gene
.
On
the
other
hand
,
P
238
L
,
G
632
A
and
G
304
R
mutations
are
the
first
cases
reported
from
Turkey
.
Our
results
indicated
that
MEFV
mutations
are
highly
heterogeneous
in
our
study
population
as
in
other
regions
of
Turkey
and
mutation
screening
techniques
such
as
PCR-RFLP
,
amplification
refractory
mutation
system
or
reverse
hybridization
do
not
adequately
detect
uncommon
or
novel
mutations
.
Therefore
,
it
was
proven
that
sequence
analysis
of
the
MEFV
gene
could
be
useful
for
detection
of
rare
or
unknown
mutations
.
Diseases
Validation
Diseases presenting
"that mefv mutations"
symptom
familial mediterranean fever
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