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Dentinogenesis imperfecta: a review and case report of a family over four generations.
[dentinogenesis imperfecta]
Dentinogenesis
imperfecta
(
DGI
)
is
one
of
the
most
common
hereditary
disorders
of
dentin
formation
.
It
follows
an
autosomal
dominant
pattern
of
transmission
,
affecting
both
the
formation
and
mineralization
of
dentin
.
Either
or
both
primary
and
permanent
dentition
is
affected
by
it
.
This
paper
briefly
reviews
the
manifestations
of
DGI
Type
II
(
DGI
1
)
and
presents
a
case
report
of
a
family
affected
with
DGI
1
over
four
generations
.