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Craniofacial morphological changes of familial bilateral hypodontia of maxillary premolars.
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The
hypodontia
of
a
permanent
tooth
from
a
dental
group
represents
a
normal
evolution
in
human
dentition
morphology
.
Nevertheless
,
the
hypodontia
of
two
teeth
within
a
dental
group
is
a
rare
developmental
anomaly
when
not
associated
to
a
systemic
syndrome
.
The
aim
of
this
study
was
to
report
two
rare
cases
of
four
maxillary
premolars
hypodontia
,
not
including
the
third
molar
,
of
two
white
women
from
the
same
family
.
There
were
presented
clinical
,
radiological
and
genetic
findings
.
These
cases
are
of
interest
to
practitioners
for
four
aspects
:
the
atypical
phenotype
of
hypodontia
,
the
complexity
of
craniofacial
morphological
changes
,
the
autosomal
dominant
familial
inheritance
with
variable
expressivity
and
the
difficult
classification
of
diagnosis
.
