Rare Diseases Symptoms Automatic Extraction
Home
A random Abstract
Our Project
Our Team
Radiographic manifestations of the temporomandibular joint in a case of Proteus syndrome.
[proteus syndrome]
Proteus
syndrome
is
a
rare
disorder
with
progressive
asymmetrical
and
disproportionate
overgrowth
of
various
tissues
of
the
body
.
The
syndrome
is
characterized
by
a
wide
range
of
malformations
,
including
craniofacial
deformities
.
Extraoral
examination
revealed
several
of
the
classical
craniofacial
features
of
Proteus
syndrome
:
pronounced
hemifacial
hypertrophy
,
macrodactyly
and
hyperostosis
.
Intraoral
examination
revealed
a
high
arched
palate
and
gingival
hyperplasia
.
Other
findings
were
unilateral
enlargement
of
the
tongue
,
alveolar
growth
and
dilaceration
of
the
roots
of
the
teeth
.
There
were
severe
degenerative
changes
and
deformities
in
the
left
temporomandibular
joint
but
the
oversized
condyle
was
asymptomatic
;
there
was
no
pain
,
limitation
and
deviation
at
mouth
opening
.
Treatment
was
not
necessary
owing
to
the
asymptomatic
situation
but
periodic
follow-up
with
clinical
and
radiographic
examination
was
considered
.
The
aim
of
this
article
is
to
describe
the
radiographic
manifestations
of
an
asymptomatic
condyle
malformation
and
other
craniofacial
,
oral
and
dental
findings
in
a
33
-
year
-old
female
patient
with
known
Proteus
syndrome
.
Diseases
Validation
Diseases presenting
"pain"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
adrenomyeloneuropathy
aniridia
aromatase deficiency
carcinoma of the gallbladder
cholangiocarcinoma
coats disease
congenital diaphragmatic hernia
congenital toxoplasmosis
cushing syndrome
cutaneous mastocytosis
cystinuria
dedifferentiated liposarcoma
dentin dysplasia
dracunculiasis
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
fabry disease
familial mediterranean fever
focal myositis
hirschsprung disease
hodgkin lymphoma, classical
holt-oram syndrome
junctional epidermolysis bullosa
kabuki syndrome
kindler syndrome
lamellar ichthyosis
liposarcoma
locked-in syndrome
lymphangioleiomyomatosis
malignant atrophic papulosis
neuralgic amyotrophy
oligodontia
oral submucous fibrosis
papillon-lefèvre syndrome
phenylketonuria
pleomorphic liposarcoma
primary hyperoxaluria type 1
proteus syndrome
pyomyositis
scrub typhus
sneddon syndrome
systemic capillary leak syndrome
thoracic outlet syndrome
trochlear dysplasia
typhoid
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
wolf-hirschhorn syndrome
This symptom has already been validated