Rare Diseases Symptoms Automatic Extraction
Home
A random Abstract
Our Project
Our Team
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
"bone marrow cells"
symptom
aromatase deficiency
erythropoietic protoporphyria
kindler syndrome
monosomy 21
You can validate or delete this automatically detected symptom
Validate the Symptom
Delete the Symptom