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Hypochondroplasia in a child with 1620C>G (Asn540Lys) mutation in FGFR3.
[achondroplasia]
Hypochondroplasia
(
HCP
)
is
an
autosomal
dominant
skeletal
dysplasia
characterized
by
short
extremities
,
short
stature
and
lumbar
lordosis
,
usually
exhibiting
a
phenotype
similar
to
but
milder
than
achondroplasia
(
ACP
)
.
Fibroblast
growth
factor
receptor
3
gene
(
FGFR
3
)
mutations
in
the
germline
are
well-known
causes
of
skeletal
syndromes
.
FGFR
3
is
a
negative
regulator
of
bone
growth
and
all
mutations
in
FGFR
3
are
gain-of-function
mutations
that
lead
to
skeletal
dysplasias
.
We
report
a
child
who
presented
with
short
stature
,
a
relatively
long
trunk
,
short
legs
,
short
arm
span
,
radiographic
evidence
of
HCP
and
mild
mental
retardation
.
Genetic
analysis
revealed
a
heterozygous
1620
C
>
G
(
Asn
540
L
ys
)
mutation
in
FGFR
3
.
To
our
knowledge
,
ours
is
the
first
case
report
of
HCP
with
a
heterozygous
1620
C
>
G
(
Asn
540
L
ys
)
mutation
in
Turkey
.
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