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Children with short-limbed short stature in pediatric endocrinological services in Japan.
[achondroplasia]
Short
-limbed
short
stature
is
a
heterogeneous
condition
that
can
reflect
the
effects
of
many
diseases
such
as
bone
disorders
,
metabolic
diseases
,
and
multiple
malformation
syndromes
.
We
conducted
a
questionnaire
survey
of
council
members
of
the
Japanese
Society
of
Pediatric
Endocrinology
and
doctors
of
our
affiliated
hospitals
in
2010
to
investigate
short
-limbed
short
stature
.
Among
91
hospitals
,
responses
were
obtained
from
61
hospitals
(
67
%
response
rate
)
.
This
study
also
examined
data
of
193
short
-limbed
short
stature
patients
,
among
whom
patients
with
FGFR
3
-
related
chondrodysplasia
such
as
achondroplasia
(
n
=
109
;
56
.
5
%
)
are
found
the
most
frequently
.
Second
to
achondroplasia
patients
,
hypochondroplasia
patients
(
n
=
47
;
24
.
4
%
)
are
the
most
frequently
observed
.
Along
with
achondroplasia
and
hypochondroplasia
patients
,
31
patients
with
disorders
of
13
other
kinds
and
6
undiagnosed
patients
were
observed
in
this
study
.
Genetic
testing
for
diagnosis
of
hypochondroplasia
is
conducted
for
only
27
.
7
%
of
all
hypochondroplasia
patients
,
although
hypochondroplasia
is
a
heterogeneous
condition
caused
not
only
by
FGFR
3
gene
mutation
but
also
by
other
causes
.
We
conducted
a
genetic
analysis
of
25
patients
who
had
been
clinically
diagnosed
as
having
'
hypochondroplasia
'
.
In
these
patients
,
other
diseases
such
as
acromicric
dysplasia
,
geleophysic
dysplasia
,
and
Aarskog-
Scott
syndrome
were
included
in
addition
to
10
FGFR
3
-
related
hypochondroplasia
patients
.
Clinical
diagnosis
of
each
disorder
representing
short
-limbed
short
stature
is
difficult
.
Therefore
,
not
only
clinical
diagnosis
but
also
genetic
diagnosis
serves
an
important
role
in
the
diagnosis
of
short-
limb
short
stature
.
Diagnostic
strategies
must
be
created
for
each
disorder
.
Diseases
Validation
Diseases presenting
"multiple malformation syndromes"
symptom
achondroplasia
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