Rare Diseases Symptoms Automatic Extraction
Home
A random Abstract
Our Project
Our Team
Epidermolysis bullosa pruriginosa: further clarification of the phenotype.
[dystrophic epidermolysis bullosa]
A
defect
in
type
VII
collagen
causes
dystrophic
epidermolysis
bullosa
(
DEB
)
.
The
pruriginosa
variant
(
DEB-Pr
)
is
unique
because
its
initial
presentation
may
be
delayed
until
adolescence
or
adulthood
,
and
its
predominant
feature
is
scarring
and
pruritus
without
the
characteristic
skin
fragility
of
DEB
.
We
describe
three
families
with
multiple
affected
members
in
which
DEB-Pr
shows
an
autosomal-dominant
inheritance
pattern
.
All
affected
individuals
were
examined
,
and
three
previously
unreported
COL
7
A
1
mutations
were
identified
.
Diseases
Validation
Diseases presenting
"defect in type vii collagen"
symptom
dystrophic epidermolysis bullosa
You can validate or delete this automatically detected symptom
Validate the Symptom
Delete the Symptom