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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
"year-old male patient"
symptom
adrenal incidentaloma
adrenomyeloneuropathy
alexander disease
allergic bronchopulmonary aspergillosis
benign recurrent intrahepatic cholestasis
cadasil
coats disease
cohen syndrome
cystinuria
dentinogenesis imperfecta
erdheim-chester disease
erythropoietic protoporphyria
esophageal carcinoma
fabry disease
heparin-induced thrombocytopenia
homocystinuria without methylmalonic aciduria
hydrocephalus with stenosis of the aqueduct of sylvius
liposarcoma
malignant atrophic papulosis
monosomy 21
oligodontia
papillon-lefèvre syndrome
pendred syndrome
pleomorphic liposarcoma
triple a syndrome
waldenström macroglobulinemia
well-differentiated liposarcoma
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