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Implant-based oral rehabilitation of a variant model of type I dentinal dysplasia: A rare case report.
[dentin dysplasia]
Dentin
dysplasia
is
an
exceptionally
rare
,
autosomal-dominant
,
hereditary
condition
,
primarily
characterized
by
defective
dentin
formation
affecting
both
the
deciduous
and
permanent
dentitions
.
The
etiology
remains
imprecise
to
date
,
in
spite
of
the
numerous
hypotheses
put
forward
and
the
constant
updates
on
this
condition
.
This
case
report
of
type
I
dentin
dysplasia
exhibits
radiographic
findings
that
are
unique
and
diverse
from
the
classical
findings
of
various
subtypes
of
this
disease
reported
to
date
.
This
article
also
depicts
the
implant-based
oral
rehabilitation
of
the
young
patient
diagnosed
with
this
variant
model
of
dentin
dysplasia
type
I
.
Early
diagnosis
and
implementation
of
this
preventive
and
curative
therapy
is
vital
for
avoiding
premature
exfoliation
of
deciduous
and
permanent
dentition
and
the
associated
residual
ridge
resorption
,
thereby
overcoming
functional
and
esthetic
deficits
and
ensuring
protection
of
the
remaining
dentition
from
further
harm
.
Diseases
Validation
Diseases presenting
"dentin dysplasia"
symptom
dentin dysplasia
dentinogenesis imperfecta
oligodontia
This symptom has already been validated
