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Seckel syndrome: report of a case.
[dentin dysplasia]
An
interesting
case
of
a
seven
years
old
boy
with
a
combination
of
clinical
,
genetic
,
radiological
,
pathologic
and
dental
findings
is
presented
in
view
of
Seckel
syndrome
literature
.
General
appearance
of
the
patient
was
characterized
by
small
forehead
,
posteriorly
slanted
ears
,
slightly
beaked
nose
,
midfacial
hypoplasia
very
stunted
stature
with
microcephaly
.
He
had
borderline
mental
retardation
with
normal
motor
development
.
Class
II
dentoskeletal
pattern
with
mild
overjet
and
open
bite
,
congenitally
missing
permanent
teeth
,
microdontia
,
enamel
hypoplasia
,
taurodontism
and
dentinal
dysplasia
was
observed
according
to
the
clinical
and
radiographic
examination
.
In
conclusion
,
Seckel
syndrome
is
not
encountered
routinely
in
dental
clinics
,
this
case
illustrates
the
importance
of
dental
care
in
such
a
rare
condition
.
Diseases
Validation
Diseases presenting
"mental retardation"
symptom
achondroplasia
alexander disease
alpha-thalassemia
aniridia
aromatase deficiency
canavan disease
classical phenylketonuria
coats disease
cohen syndrome
cowden syndrome
cystinuria
dentin dysplasia
familial hypocalciuric hypercalcemia
homocystinuria without methylmalonic aciduria
hydrocephalus with stenosis of the aqueduct of sylvius
kabuki syndrome
kallmann syndrome
lamellar ichthyosis
lymphangioleiomyomatosis
monosomy 21
phenylketonuria
primary hyperoxaluria type 1
proteus syndrome
pyruvate dehydrogenase deficiency
sneddon syndrome
triple a syndrome
wolf-hirschhorn syndrome
zellweger syndrome
This symptom has already been validated