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Overview of epidermolysis bullosa.
[kindler syndrome]
Epidermolysis
bullosa
(
EB
)
is
classified
into
major
types
-
EB
simplex
(
EBS
)
,
junctional
EB
(
JEB
)
and
dystrophic
EB
(
DEB
)
-
on
the
basis
of
the
level
of
tissue
separation
within
the
cutaneous
basement
membrane
zone
.
Recent
advances
in
research
on
EB
have
led
to
the
identification
of
10
genes
responsible
for
EB
.
The
Japanese
Ministry
of
Health
,
Labor
and
Welfare
has
designated
JEB
and
DEB
,
but
not
EBS
,
as
specified
diseases
.
However
,
EBS
has
a
lethal
variant
and
should
also
be
registered
as
a
specified
disease
.
In
the
Third
Consensus
Meeting
on
the
Diagnosis
and
Classification
of
EB
held
in
Vienna
in
2007
,
it
was
recommended
that
Kindler
syndrome
should
be
classified
as
a
subtype
of
EB
.
Corrective
gene
therapy
is
the
most
ideal
therapy
for
EB
,
but
much
more
research
is
required
before
it
can
be
developed
and
used
in
clinical
practice
.
Cell-based
therapies
using
fibroblasts
and
bone
marrow
cells
have
recently
attracted
considerable
attention
.
Diseases
Validation
Diseases presenting
"attracted considerable attention"
symptom
kindler syndrome
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