Rare Diseases Symptoms Automatic Extraction
Home
A random Abstract
Our Project
Our Team
Molecular genetic analysis of a female patient with pyruvate dehydrogenase deficiency: detection of a new mutation and differential expression of mutant gene product in cultured cells.
[pyruvate dehydrogenase deficiency]
A
new
18
bp
insertion
mutation
in
the
gene
for
the
alpha
subunit
of
pyruvate
dehydrogenase
(
E
1
alpha
)
was
found
in
a
female
patient
with
congenital
lactic
acidaemia
.
Cultured
skin
fibroblasts
and
Epstein-
Barr
virus-transformed
lymphoblastoid
cells
from
this
patient
showed
decreased
and
normal
pyruvate
dehydrogenase
complex
(
PDHC
)
activity
,
respectively
.
This
18
bp
insertion
was
a
de
novo
mutation
,
because
it
was
not
present
in
her
parents
.
Although
this
female
patient
was
heterozygous
for
the
normal
and
the
mutant
alleles
,
97
%
of
cultured
skin
fibroblasts
expressed
the
mutant
allele
,
while
100
%
of
cultured
lymphoblastoid
cells
,
94
%
of
peripheral
blood
lymphocytes
and
98
%
of
IL
-
2
-
activated
T
-
cells
expressed
the
normal
allele
.
These
results
suggest
that
in
this
patient
the
X
chromosome
containing
the
normal
allele
was
predominantly
inactivated
in
fibroblasts
and
the
X
chromosome
containing
the
mutant
allele
was
predominantly
inactivated
in
lymphocytes
.
The
diagnosis
of
E
1
alpha
deficiency
is
usually
established
by
measurement
of
PDHC
activity
and
the
level
of
immunoreactive
proteins
.
However
,
these
methods
are
not
sufficient
to
diagnose
the
disorder
in
female
patients
with
E
1
alpha
deficiency
due
to
differential
inactivation
of
the
X
chromosome
.
Therefore
,
it
is
necessary
to
develop
a
new
method
to
firmly
establish
the
diagnosis
of
E
1
alpha
deficiency
.
Diseases
Validation
Diseases presenting
"skin fibroblasts"
symptom
child syndrome
cowden syndrome
cystinuria
dentinogenesis imperfecta
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
gm1 gangliosidosis
homocystinuria without methylmalonic aciduria
krabbe disease
malignant atrophic papulosis
monosomy 21
neonatal adrenoleukodystrophy
pyruvate dehydrogenase deficiency
werner syndrome
x-linked adrenoleukodystrophy
zellweger syndrome
You can validate or delete this automatically detected symptom
Validate the Symptom
Delete the Symptom