Rare Diseases Symptoms Automatic Extraction
Home
A random Abstract
Our Project
Our Team
Neonatal cutaneous mastocytosis.
[cutaneous mastocytosis]
Neonatal
cutaneous
mastocytosis
is
rare
infiltrative
disorder
of
the
skin
.
Though
often
asymptomatic
,
systemic
features
may
be
associated
with
any
clinical
pattern
of
the
disorder
at
any
age
group
.
We
present
our
experience
with
a
3
1
/
2
months
old
female
child
.
She
presented
with
recurrent
eruption
of
tense
bullae
preceded
by
flushing
,
irritability
since
day
3
of
life
.
Darier
sign
and
dermatographism
were
present
.
Skin
biopsy
confirmed
the
case
as
urticaria
pigmentosa
which
is
the
most
common
form
of
cutaneous
mastocytosis
.
Investigation
revealed
deranged
liver
function
.
Child
was
given
H
1
antihistaminics
and
topical
glucocorticoid
.
Family
counselled
about
chance
of
anaphylaxis
to
various
toxins
and
drugs
and
risk
of
development
of
systemic
mastocytosis
.
Diseases
Validation
Diseases presenting
"common form"
symptom
achondroplasia
alexander disease
benign recurrent intrahepatic cholestasis
cadasil
child syndrome
classical phenylketonuria
cutaneous mastocytosis
erythropoietic protoporphyria
familial mediterranean fever
hereditary cerebral hemorrhage with amyloidosis
hodgkin lymphoma, classical
holt-oram syndrome
homocystinuria without methylmalonic aciduria
oral submucous fibrosis
pendred syndrome
primary hyperoxaluria type 1
severe combined immunodeficiency
thoracic outlet syndrome
You can validate or delete this automatically detected symptom
Validate the Symptom
Delete the Symptom