Rare Diseases Symptoms Automatic Extraction
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The etiology of short stature affects the clinical outcome of lower limb lengthening using external fixation. A systematic review of 18 trials involving 547 patients.
[achondroplasia]
Distraction
osteogenesis
(
DO
)
has
been
used
to
gain
height
in
short
statured
individuals
.
However
,
there
have
been
no
studies
comparing
the
clinical
outcome
of
limb
lengthening
based
on
the
etiology
of
the
short
stature
.
We
assessed
whether
different
underlying
diagnoses
are
associated
with
varied
clinical
outcomes
in
these
patients
.
We
performed
a
systematic
review
of
the
literature
pertaining
to
lower
limb
lengthening
using
external
fixation
for
short
stature
.
Clinical
outcomes
including
amount
of
lengthening
,
healing
index
(
HI
)
,
and
complications
based
on
the
underlying
diagnosis
for
the
short
stature
were
documented
.
18
clinical
studies
were
included
,
with
547
patients
who
underwent
1
,
581
lower
limb
segment
lengthening
procedures
.
Mean
follow-up
was
4
.
3
years
.
The
average
age
at
lengthening
was
less
for
individuals
with
achondroplasia
/
hypochondroplasia
(
A
/
H
)
(
14
.
5
years
)
than
for
those
with
Turner
's
syndrome
(
TS
)
(
18
.
2
years
)
or
with
constitutional
short
stature
(
CSS
)
(
21
.
7
years
)
.
Mean
height
gained
was
greater
in
patients
with
A
/
H
(
9
.
5
cm
)
than
in
those
with
TS
(
7
.
7
cm
)
or
CSS
(
6
.
1
cm
)
group
.
The
HI
was
better
in
A
/
H
(
30
.
8
days
/
cm
)
and
CSS
(
32
days
/
cm
)
than
in
TS
(
45
.
1
days
/
cm
)
.
The
reported
complication
rate
per
segment
was
lower
for
A
/
H
(
0
.
68
)
and
TS
(
0
.
71
)
than
for
CSS
(
1
.
06
)
.
Patients
with
A
/
H
tolerated
larger
amounts
of
lengthening
with
fewer
complications
than
those
with
other
diagnoses
.
Diseases
Validation
Diseases presenting
"short stature"
symptom
22q11.2 deletion syndrome
achondroplasia
alpha-thalassemia
aromatase deficiency
child syndrome
classical phenylketonuria
coats disease
cohen syndrome
congenital adrenal hyperplasia
cowden syndrome
dentin dysplasia
dentinogenesis imperfecta
fabry disease
hirschsprung disease
holt-oram syndrome
kabuki syndrome
kallmann syndrome
kindler syndrome
monosomy 21
oculocutaneous albinism
oligodontia
omenn syndrome
proteus syndrome
werner syndrome
wolf-hirschhorn syndrome
zellweger syndrome
This symptom has already been validated