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Dentinal dysplasia type I: a case report with a 6-year followup.
[dentin dysplasia]
Introduction
.
Dentin
dysplasia
is
a
rare
disturbance
of
dentin
formation
characterized
by
normal
enamel
but
atypical
dentin
formation
with
abnormal
pulpal
morphology
that
is
inherited
as
an
autosomal
pulpal
morphology
.
Case
Presentation
.
A
7
-
year
-old
female
who
had
problems
in
chewing
function
was
referred
to
Oral
and
Maxillofacial
Surgery
Department
at
the
Faculty
of
Dentistry
in
Ondokuz
Mayıs
University
.
In
the
radiographic
examination
,
it
was
determined
that
some
of
the
unerupted
permanent
teeth
of
the
patient
had
short
,
blunted
,
and
malformed
roots
with
obliterated
pulp
chambers
,
although
the
bone
below
the
teeth
showed
well-defined
margins
.
This
unusual
case
of
generalized
short
roots
presents
a
case
demonstrating
both
classic
and
atypical
features
of
dentinal
dysplasia
type
I
(
DDI
)
in
the
mixed
and
permanent
dentitions
.
Conclusion
.
There
are
still
many
issues
in
the
diagnosis
and
management
of
patients
with
dentin
dysplasia
.
Early
diagnosis
,
clinical
and
radiographic
findings
,
as
well
as
treatment
of
this
condition
and
the
initiation
of
effective
preventive
strategies
may
help
prevent
or
delay
loss
of
dentition
.
Diseases
Validation
Diseases presenting
"atypical features"
symptom
dentin dysplasia
hodgkin lymphoma, classical
holt-oram syndrome
kabuki syndrome
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