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A Japanese-specific recurrent mutation and a novel splice site mutation in the LAMC2 gene identified in two Japanese families with Herlitz junctional epidermolysis bullosa.
[junctional epidermolysis bullosa]
Herlitz
junctional
epidermolysis
bullosa
(
H-
JEB
)
is
an
extremely
rare
genodermatosis
characterized
by
lethality
owing
to
severe
blister
formation
.
We
report
two
unrelated
Japanese
patients
with
H-
JEB
.
Genetic
analyses
detected
a
single
nonsense
mutation
on
the
LAMC
2
gene
in
these
two
patients
.
To
identify
the
mutation
involved
and
describe
the
first
reported
Japanese
recurrent
mutation
in
the
LAMC
2
gene
.
Direct
sequencing
was
performed
of
DNA
from
either
peripheral
blood
or
fetal
cells
in
amniotic
fluid
.
Reverse
transcriptase
PCR
was
used
to
confirm
that
an
aberrant
transcript
resulted
from
the
splice
site
mutation
.
A
haplotype
analysis
was
performed
to
define
the
origin
of
the
recurrent
mutation
.
Both
patients
had
blisters
and
erosions
on
the
trunk
and
limbs
at
birth
,
with
nail
dystrophy
.
Patient
1
died
as
a
result
of
sepsis
at
30
weeks
of
age
,
and
patient
2
died
as
a
result
of
disseminated
intravascular
coagulation
at
20
weeks
of
age
.
Mutation
analysis
of
the
LAMC
2
gene
revealed
that
patient
1
was
compound
heterozygous
for
a
nonsense
mutation
(
p
.
Cys
553
X
)
and
a
novel
splice
site
mutation
(
c
.
2868
+
1
delG
)
,
and
patient
2
was
a
homozygous
for
p
.
Cys
553
X
.
Prenatal
diagnosis
performed
during
a
subsequent
pregnancy
in
family
2
revealed
that
this
second
child
was
heterozygous
for
p
.
Cys
553
X
,
and
was
thus
not
affected
.
Haplotype
analysis
suggested
that
a
p
.
Cys
553
X
allele
derived
from
the
same
origin
had
been
independently
inherited
by
these
two
unrelated
families
.
p
.
Cys
553
X
in
the
LAMC
2
gene
may
be
a
Japanese
-
specific
recurrent
mutation
as
a
result
of
a
founder
effect
,
and
it
may
therefore
be
useful
for
initial
screening
in
the
mutation
analysis
of
H-
JEB
.
Diseases
Validation
Diseases presenting
"disseminated intravascular coagulation at 20 weeks of age"
symptom
junctional epidermolysis bullosa
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