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Influence of dietary iodine deficiency on the thyroid gland in Slc26a4-null mutant mice.
[pendred syndrome]
Pendred
syndrome
(
PDS
)
is
an
autosomal
recessive
disorder
characterized
by
sensorineural
hearing
impairment
and
variable
degree
of
goitrous
enlargement
of
the
thyroid
gland
with
a
partial
defect
in
iodine
organification
.
The
thyroid
function
phenotype
can
range
from
normal
function
to
overt
hypothyroidism
.
It
is
caused
by
loss
-of-function
mutations
in
the
SLC
26
A
4
(
PDS
)
gene
.
The
severity
of
the
goiter
has
been
postulated
to
depend
on
the
amount
of
dietary
iodine
intake
.
However
,
direct
evidence
has
not
been
shown
to
support
this
hypothesis
.
Because
Slc
26
a
4
-
null
mice
have
deafness
but
do
not
develop
goiter
,
we
fed
the
mutant
mice
a
control
diet
or
an
iodine-
deficient
diet
to
evaluate
whether
iodine
deficiency
is
a
causative
environmental
factor
for
goiter
development
in
PDS
.
We
evaluated
the
thyroid
volume
in
histological
sections
with
the
use
of
three
-dimensional
reconstitution
software
,
we
measured
serum
levels
of
total
tri
-iodothyronine
(
TT
3
)
and
total
thyroxine
(
TT
4
)
levels
,
and
we
studied
the
thyroid
gland
morphology
by
transmission
electron
microscopy
.
TT
4
levels
became
low
but
TT
3
levels
did
not
change
significantly
after
eight
weeks
of
an
iodine-
deficient
diet
compared
to
levels
in
the
control
diet
animals
.
Even
in
Slc
26
a
4
-
null
mice
fed
an
iodine-
deficient
diet
,
the
volume
of
the
thyroid
gland
did
not
increase
although
the
size
of
each
epithelial
cell
increased
with
a
concomitant
decrease
of
thyroid
colloidal
area
.
An
iodine-
deficient
diet
did
not
induce
goiter
in
Slc
26
a
4
-
null
mice
,
suggesting
that
other
environmental
,
epigenetic
or
genetic
factors
are
involved
in
goiter
development
in
PDS
.
Diseases
Validation
Diseases presenting
"thyroid gland morphology"
symptom
pendred syndrome
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