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Sneddon syndrome associated with Protein S deficiency.
[sneddon syndrome]
Sneddon
syndrome
(
SS
)
is
rare
,
arterio-occlusive
disorder
characterized
by
generalized
livedo
racemosa
of
the
skin
and
various
central
nervous
symptoms
due
to
occlusion
of
medium-sized
arteries
of
unknown
.
Seizure
,
cognitive
impairment
,
hypertension
,
and
history
of
repetitive
miscarriages
are
the
other
symptoms
seen
in
this
disease
.
Livedo
racemosa
involves
persisting
irreversible
skin
lesions
red
or
blue
in
color
with
irregular
margins
.
Usually
,
SS
occurs
in
women
of
childbearing
age
.
Protein
S
deficiency
is
an
inherited
or
acquired
disorder
associated
with
an
increased
risk
of
thrombosis
.
We
present
a
33
-
year
-old
woman
with
SS
with
diffuse
livedo
racemosa
,
recurrent
cerebrovascular
diseases
,
migraine
-
type
headache
,
sinus
vein
thrombosis
,
and
protein
S
deficiency
.
Protein
S
deficiency
and
with
Sneddon
syndrome
rarely
encountered
in
the
literature
.
Diseases
Validation
Diseases presenting
"seizure"
symptom
alexander disease
canavan disease
cohen syndrome
cowden syndrome
homocystinuria without methylmalonic aciduria
hydrocephalus with stenosis of the aqueduct of sylvius
kabuki syndrome
neonatal adrenoleukodystrophy
pendred syndrome
pyruvate dehydrogenase deficiency
sneddon syndrome
wolf-hirschhorn syndrome
This symptom has already been validated