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achondroplAsia
英音[ eɪˌkɒndrəˈpleɪzɪə ] 美音[ eɪˌkɑːndrəˈpleɪʒə ]
[外科] 软骨发育不全
常用释义
词性释义
n.
[外科] 软骨发育不全
例句
全部
In
this
study
,
researchers
found
a
connection
between a
mutation
in
sperm
DNA
and
a form
of
dwarfism
known as
achondroplasia
.
在这个研究中，研究者发现精子DNA变异和侏儒症（软骨发育不全）存在联系。
Their
newborn
daughter
died
last year
from
a
devastating
dwarfism
-
related
disease
called
homozygous
achondroplasia
.
他们的新生女儿去年死于一种破坏性很强的侏儒相关性疾病，叫做纯合软骨发育不良。
I
stand
three
feet
,
nine
inches
tall
.
I
am an
achondroplasia
dwarf
,
which
is
a
person
having
very
short
limbs
.
我只有三英尺九英寸高，是一个患软骨发育不全症的侏儒，四肢短小。
The
teenager
,
who
is
the
world
's
smallest
girl
according
to the
Indian
Book of
Records
,
has a
form
of
dwarfism
called
achondroplasia
.
根据《印度记录》，这个花季少女是世界上身材最矮小的人，她的这种病症被称作软骨发育不全。
Objective
: To
study
the
clinical
, sonographic,
radiographic
and
pathologic
characteristics
of
achondroplasia
.
目的研究软骨发育不全的临床、影像学和病理学表现。
Genetical
diagnosis
in
a
congenital
achondroplasia
family
先天性软骨发育不全一家系的基因诊断
Hereditary
dwarfisms
include
achondroplAsia
,
with
normal
trunk
size
But
short
limbs
and
a
large
head
;
遗传性侏儒症包括︰软骨发育不全，躯干发育正常，但肢体极短，头较大；
Mutation
analysis
of
fibroblast
growth
factor
receptor
3
gene
in
an
achondroplasia
family
一个软骨发育不全家系成纤维细胞生长因子受体3基因突变分析
Detection
of fibroblast
growth
factor
receptor
3
gene
mutation
at
nucleotide
1138
site
in
congenital
achondroplasia
patients
先天性软骨发育不全成纤维细胞生长因子受体3基因1138位核苷酸点突变的检测
Ultrasonic
diagnosis
of
fetus
achondroplasia
(
analysis
of
7
cases
)
胎儿软骨发育不全的超声诊断（附7例分析）