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Dentin dysplasia type I.
[dentin dysplasia]
Dentin
dysplasia
type
I
is
a
rare
hereditary
disturbance
of
dentin
formation
characterised
clinically
by
nearly
normal
appearing
crowns
and
hypermobility
of
teeth
that
affects
one
in
every
100
,
000
individuals
and
manifests
in
both
primary
and
permanent
dentitions
.
Radiographic
analysis
shows
obliteration
of
all
pulp
chambers
,
short
,
blunted
,
and
malformed
roots
,
and
periapical
radiolucencies
of
non-
carious
teeth
.
This
paper
presents
three
cases
demonstrating
classic
features
of
type
I
dentin
dysplasia
.
Diseases
Validation
Diseases presenting
"dentin dysplasia"
symptom
dentin dysplasia
dentinogenesis imperfecta
oligodontia
This symptom has already been validated