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Cutaneous mastocytosis associated with congenital alopecia.
[cutaneous mastocytosis]
Mastocytosis
is
a
rare
disorder
that
shows
accumulation
of
mast
cells
in
tissues
.
Atypical
clinical
features
may
mimic
impetigo
,
Langerhans
cell
histiocytosis
,
and
carcinoid
syndrome
;
however
,
only
1
case
of
scarring
alopecia
associated
with
mastocytosis
has
been
reported
.
We
present
the
first
case
of
cutaneous
mastocytosis
associated
with
congenital
alopecia
areata
in
a
3
-
year
-old
Korean
girl
.
This
case
showed
an
atypical
clinical
presentation
of
congenital
alopecia
areata
,
but
histopathological
results
confirmed
the
diagnosis
of
cutaneous
mastocytosis
.
Diseases
Validation
Diseases presenting
"first case"
symptom
achondroplasia
adrenal incidentaloma
allergic bronchopulmonary aspergillosis
alpha-thalassemia
aniridia
aromatase deficiency
canavan disease
carcinoma of the gallbladder
child syndrome
cholangiocarcinoma
classical phenylketonuria
coats disease
cohen syndrome
congenital toxoplasmosis
cushing syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dentin dysplasia
dracunculiasis
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
esophageal adenocarcinoma
esophageal carcinoma
fabry disease
familial mediterranean fever
focal myositis
gm1 gangliosidosis
harlequin ichthyosis
hodgkin lymphoma, classical
homocystinuria without methylmalonic aciduria
junctional epidermolysis bullosa
kabuki syndrome
krabbe disease
lamellar ichthyosis
legionellosis
liposarcoma
locked-in syndrome
malignant atrophic papulosis
monosomy 21
neonatal adrenoleukodystrophy
oculocutaneous albinism
omenn syndrome
papillon-lefèvre syndrome
pendred syndrome
pleomorphic liposarcoma
primary effusion lymphoma
primary hyperoxaluria type 1
proteus syndrome
pyomyositis
systemic capillary leak syndrome
thoracic outlet syndrome
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
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