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Diagnosis and management of extensive vascular malformations of the lower limb: part I. Clinical diagnosis.
[proteus syndrome]
There
is
significant
confusion
in
the
literature
when
describing
vascular
anomalies
,
and
vascular
malformations
are
often
misnamed
or
incorrectly
classified
.
Part
I
of
this
two
-part
series
on
the
diagnosis
and
management
of
extensive
vascular
malformations
of
the
lower
limbs
will
discuss
the
dermatologist
's
role
in
the
diagnosis
of
these
lesions
.
At
least
nine
types
of
vascular
malformations
with
specific
clinical
and
radiologic
characteristics
must
be
distinguished
in
the
lower
limbs
:
Klippel-
Trénaunay
syndrome
,
port-wine
stain
with
or
without
hypertrophy
,
cutis
marmorata
telangiectatica
congenita
,
macrocephaly
-capillary
malformation
,
Parkes
Weber
syndrome
,
Stewart
-
Bluefarb
syndrome
,
venous
malformation
,
glomuvenous
malformation
,
and
lymphatic
malformation
.
This
article
highlights
the
differences
in
clinical
appearance
and
discusses
the
differential
diagnosis
of
extensive
vascular
malformations
in
an
attempt
to
ensure
earlier
diagnosis
and
better
outcomes
for
these
patients
.
Diseases
Validation
Diseases presenting
"macrocephaly-capillary malformation"
symptom
proteus syndrome
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