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Candidate-gene exclusion in a family with inherited non-syndromic dental disorders.
[dentinogenesis imperfecta]
Amelogenesis
imperfecta
,
dentinogenesis
imperfecta
,
and
dentin
dysplasia
are
the
most
common
non-syndromic
dental
disorders
.
In
this
study
,
we
analysed
and
localised
the
gene
(
s
)
responsible
for
inherited
non-syndromic
dental
disorders
in
a
Chinese
family
.
This
study
identified
and
researched
non-syndromic
dental
disorders
in
a
four
-generation
Chinese
family
,
including
four
affected
individuals
whose
clinical
phenotype
was
atypical
.
Linkage
analysis
with
seven
polymorphic
markers
that
localise
to
six
different
autochromosomes
showed
that
the
family
was
linked
through
chromosome
4
q
.
All
exons
and
exon-intron
boundaries
of
dentin
sialophosphoprotein
(
DSPP
)
,
enamelin
(
ENAM
)
,
and
ameloblastin
(
AMBN
)
,
which
are
located
on
chromosome
4
q
,
were
sequenced
in
nine
of
the
family
members
.
Direct
DNA
sequence
analysis
revealed
the
existence
of
a
G
to
A
transversion
in
exon
4
(
g
.
13081786
G
>
A
,
c
.
727
G
>
A
,
p
.
Asp
243
Asn
,
based
on
reference
sequences
NM
_
014208
.
3
)
of
the
DSPP
gene
,
and
this
sequence
variation
correlated
exactly
with
the
presence
of
the
disease
.
These
results
indicate
that
mutation
p
.
A
sp
243
A
sn
is
a
highly
probable
cause
of
non-syndromic
dental
disorder
in
this
Chinese
family
.
The
presence
of
symptom
heterogeneity
is
possible
,
as
the
clinical
classification
system
is
hampered
by
the
lack
of
close
correlation
between
the
subtype
and
the
molecular
defect
.
Diseases
Validation
Diseases presenting
"the molecular defect"
symptom
dentin dysplasia
dentinogenesis imperfecta
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