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Live birth following preimplantation genetic screening for trisomy 21. Should aneuploidy screening be offered to all older patients undergoing IVF?
[monosomy 21]
A
42
-
year
-old
female
patient
with
history
of
secondary
infertility
was
referred
to
our
assisted
conception
unit
for
in
vitro
fertilization
(
IVF
)
.
Before
her
referral
,
she
had
two
cycles
of
IVF
at
another
centre
;
the
first
was
unsuccessful
and
,
after
conceiving
at
the
second
attempt
,
the
pregnancy
was
terminated
at
14
weeks
'
gestation
following
a
positive
nuchal
translucency
scan
and
a
diagnosis
of
trisomy
21
(
Down
syndrome
)
by
a
chorionic
villous
biopsy
performed
in
the
first
trimester
.
The
screening
tests
for
trisomy
21
were
offered
to
the
patient
in
view
of
her
advanced
age
.
Subsequent
karyotyping
revealed
that
both
partners
had
a
normal
chromosomal
complement
.
Following
genetic
counselling
,
the
couple
were
offered
IVF
treatment
along
with
preimplantation
genetic
screening
for
trisomy
21
.
Four
of
the
five
embryos
were
suitable
for
biopsy
,
and
one
blastomere
from
each
embryo
was
analyzed
using
fluorescent
in
situ
hybridization
for
chromosome
21
.
The
analysis
revealed
that
two
embryos
had
trisomy
21
,
one
had
monosomy
21
,
and
only
one
embryo
was
diploid
for
chromosome
21
.
The
single
diploid
embryo
was
transferred
to
the
uterus
on
day
3
,
and
resulted
in
an
uneventful
pregnancy
and
delivery
of
a
healthy
live-born
male
.
Diseases
Validation
Diseases presenting
"year-old female patient"
symptom
adrenal incidentaloma
aniridia
benign recurrent intrahepatic cholestasis
cowden syndrome
cushing syndrome
epidermolysis bullosa simplex
esophageal squamous cell carcinoma
holt-oram syndrome
krabbe disease
lamellar ichthyosis
liposarcoma
lymphangioleiomyomatosis
malignant atrophic papulosis
monosomy 21
neuralgic amyotrophy
oculocutaneous albinism
oligodontia
oral submucous fibrosis
proteus syndrome
pyomyositis
sneddon syndrome
thoracic outlet syndrome
triple a syndrome
von hippel-lindau disease
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