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Partial lipodystrophy with severe insulin resistance and adult progeria Werner syndrome.
[werner syndrome]
Laminopathies
,
due
to
mutations
in
LMNA
,
encoding
A
type
-lamins
,
can
lead
to
premature
ageing
and
/
or
lipodystrophic
syndromes
,
showing
that
these
diseases
could
have
close
physiopathological
relationships
.
We
show
here
that
lipodystrophy
and
extreme
insulin
resistance
can
also
reveal
the
adult
progeria
Werner
syndrome
linked
to
mutations
in
WRN
,
encoding
a
RecQ
DNA
helicase
.
We
analysed
the
clinical
and
biological
features
of
two
women
,
aged
32
and
36
,
referred
for
partial
lipodystrophic
syndrome
which
led
to
the
molecular
diagnosis
of
Werner
syndrome
.
Cultured
skin
fibroblasts
from
one
patient
were
studied
.
Two
normal-weighted
women
presented
with
a
partial
lipodystrophic
syndrome
with
hypertriglyceridemia
and
liver
steatosis
.
One
of
them
had
also
diabetes
.
Both
patients
showed
a
peculiar
,
striking
lipodystrophic
phenotype
with
subcutaneous
lipoatrophy
of
the
four
limbs
contrasting
with
truncal
and
abdominal
fat
accumulation
.
Their
oral
glucose
tolerance
tests
showed
extremely
high
levels
of
insulinemia
,
revealing
major
insulin
resistance
.
Low
serum
levels
of
sex-hormone
binding
globulin
and
adiponectin
suggested
a
post-receptor
insulin
signalling
defect
.
Other
clinical
features
included
bilateral
cataracts
,
greying
hair
and
distal
skin
atrophy
.
We
observed
biallelic
WRN
null
mutations
in
both
women
(
p
.
Q
748
X
homozygous
,
and
compound
heterozygous
p
.
Q
1257
X
/
p
.
M
1329
fs
)
.
Their
fertility
was
decreased
,
with
preserved
menstrual
cycles
and
normal
follicle-stimulating
hormone
levels
ruling
out
premature
ovarian
failure
.
However
undetectable
anti-müllerian
hormone
and
inhibin
B
indicated
diminished
follicular
ovarian
reserve
.
Insulin
-resistance
linked
ovarian
hyperandrogenism
could
also
contribute
to
decreased
fertility
,
and
the
two
patients
became
pregnant
after
initiation
of
insulin
-sensitizers
(
metformin
)
.
Both
pregnancies
were
complicated
by
severe
cervical
incompetence
,
leading
to
the
preterm
birth
of
a
healthy
newborn
in
one
case
,
but
to
a
second
trimester-abortion
in
the
other
.
WRN
-mutated
fibroblasts
showed
oxidative
stress
,
increased
lamin
B
1
expression
,
nuclear
dysmorphies
and
premature
senescence
.
We
show
here
for
the
first
time
that
partial
lipodystrophy
with
severe
insulin
resistance
can
reveal
WRN
-linked
premature
aging
syndrome
.
Increased
expression
of
lamin
B
1
with
altered
lamina
architecture
observed
in
WRN
-mutated
fibroblasts
could
contribute
to
premature
cellular
senescence
.
Primary
alterations
in
DNA
replication
and
/
or
repair
should
be
considered
as
possible
causes
of
lipodystrophic
syndromes
.
Diseases
Validation
Diseases presenting
"leading to the preterm birth of a healthy newborn in one case"
symptom
werner syndrome
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