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Management of craniofacial hyperostosis in Proteus syndrome.
[proteus syndrome]
Proteus
syndrome
is
a
rare
congenital
hamartomatous
condition
that
is
characterized
by
a
wide
range
of
malformations
,
occasionally
involving
the
head
and
the
face
.
Skin
and
skeletal
developmental
malformations
are
common
and
may
be
manifested
in
significant
physical
anomalies
.
In
this
report
,
we
describe
the
cases
of
2
patients
affected
by
this
condition
.
For
one
patient
,
a
recurrence
occurred
4
years
after
the
elimination
of
cranial
hyperostosis
.
In
the
second
patient
,
although
we
observed
macrosomia
and
peculiar
countenance
in
the
context
of
craniofacial
hyperostosis
,
the
patient
did
not
visit
a
clinic
for
approximately
50
years
before
seeking
treatment
.
The
management
of
the
craniofacial
involvement
is
described
,
and
a
literature
overview
is
presented
.
Diseases
Validation
Diseases presenting
"wide range"
symptom
22q11.2 deletion syndrome
acute rheumatic fever
adrenomyeloneuropathy
alexander disease
allergic bronchopulmonary aspergillosis
alpha-thalassemia
aromatase deficiency
benign recurrent intrahepatic cholestasis
cadasil
carcinoma of the gallbladder
congenital toxoplasmosis
cowden syndrome
cystinuria
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erdheim-chester disease
fabry disease
gm1 gangliosidosis
harlequin ichthyosis
homocystinuria without methylmalonic aciduria
hydrocephalus with stenosis of the aqueduct of sylvius
legionellosis
neonatal adrenoleukodystrophy
oral submucous fibrosis
pendred syndrome
phenylketonuria
pleomorphic liposarcoma
primary effusion lymphoma
primary hyperoxaluria type 1
proteus syndrome
pyruvate dehydrogenase deficiency
scrub typhus
systemic capillary leak syndrome
thoracic outlet syndrome
triple a syndrome
trochlear dysplasia
well-differentiated liposarcoma
werner syndrome
x-linked adrenoleukodystrophy
zellweger syndrome
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