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Neural tube defects and atypical deletion on 22q11.2.
[22q11.2 deletion syndrome]
The
22
q
11
.
2
deletion
syndrome
(
22
q
11
.
2
DS
)
is
a
common
microdeletion
disorder
.
Most
of
the
patients
show
the
common
3
 
Mb
deletion
but
proximal
1
.
5
 
Mb
deletion
and
unusual
deletions
located
outside
the
common
deleted
region
,
have
been
detected
particularly
with
the
advance
of
comparative
cytogenomic
microarray
technologies
.
The
individuals
reported
in
the
literature
with
unusual
deletions
involving
the
22
q
11
region
,
showed
milder
facial
phenotypes
,
decreased
incidence
of
cardiac
anomalies
,
and
intellectual
disability
.
We
describe
two
sibs
with
an
atypical
0
.
8
 
Mb
microdeletion
of
chromosome
22
q
11
who
both
showed
myelomeningocele
and
mild
facial
dysmorphisms
.
The
association
between
neural
tube
defect
and
the
clinical
diagnosis
of
Di
George
anomaly
/
velocardiofacial
syndrome
is
well
documented
in
the
literature
,
but
not
all
cases
had
molecular
studies
to
determine
breakpoint
regions
.
This
report
helps
to
narrow
a
potential
critical
region
for
neural
tube
defects
associated
with
22
q
11
deletions
.
©
2014
Wiley
Periodicals
,
Inc
.
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"potential critical region"
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22q11.2 deletion syndrome
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