Rare Diseases Symptoms Automatic Extraction
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Famlial nonsyndromic oligodontia.
[oligodontia]
Oligodontia
is
one
of
the
most
common
developmental
abnormalities
in
humans
.
The
present
case
report
highlights
the
features
of
oligodontia
in
a
12
-
year
-old
male
patient
which
was
managed
successfully
with
multidisciplinary
approach
.
Familial
oligodontia
represents
as
an
absence
of
varying
numbers
of
secondary
teeth
seen
as
an
isolated
trait
.
The
advance
in
the
understanding
of
tooth
development
and
genetic
control
of
tooth
morphology
not
only
allows
clinical
research
to
broaden
the
knowledge
of
tooth
agenesis
but
also
provides
optimum
clinical
care
.
Diseases
Validation
Diseases presenting
"common developmental abnormalities in humans"
symptom
oligodontia
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