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Dentin dysplasia type I: a case report and review of the literature.
[dentin dysplasia]
Dentin
dysplasia
is
a
rare
hereditary
disturbance
of
dentin
formation
characterized
by
defective
dentin
development
with
clinically
normal
appearing
crowns
,
severe
hypermobility
of
teeth
and
spontaneous
dental
abscesses
or
cysts
.
Radiographic
analysis
shows
obliteration
of
all
pulp
chambers
,
short
,
blunted
and
malformed
or
absent
roots
and
peri-apical
radiolucencies
of
non
carious
teeth
.
We
present
a
case
of
dentin
dysplasia
type
I
in
a
12
-
year
-old
Iranian
boy
,
and
the
clinical
,
radiographic
and
histopathologic
findings
of
this
condition
and
treatment
are
described
.
There
are
still
many
inconclusive
issues
in
the
diagnosis
and
management
of
patients
with
dentin
dysplasia
.
The
diagnostic
features
of
this
rare
disturbance
will
remain
incompletely
defined
until
additional
cases
have
been
described
.
Early
diagnosis
of
the
condition
and
initiation
of
effective
regular
dental
treatments
may
help
these
patients
to
prevent
or
delay
loss
of
dentition
.
Diseases
Validation
Diseases presenting
"initiation of effective regular dental treatments may help these patients to prevent or delay loss of dentition"
symptom
dentin dysplasia
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