发育不全

The children of a person who has achondroplasia have a 50% hance of inheriting the condition;75% of people with achondroplasia are born to parents who do not have the condition.

软骨发育不全症患者的后代有50%的几率会继承这种疾病状况，75%的软骨发育不全症患者的父母没有这种疾病状况。

Of, relating to, or characterized by aplasia .

发育不全的发育不全的，有关发育不全的或以发育不全为特点的

The axial rotation of the earth.Of, relating to, or characterized by aplasia .

发育不全的发育不全的，有关发育不全的或以发育不全为特点的

Additional findings can include synkinesia of the digits, unilateral renal agenesis, sensorineural hearing loss, cleft lip and/or palate, agenesis of one or more teeth, brachydactyly, syndactyly, and agenesis of the corpus callosum.

其他表现可包括手指联带运动、单侧肾脏发育不全、感音性听力丧失、裂唇和/或裂腭、一个或多个牙齿发育不全、短指、并指以及胼胝体发育不全。

Methods Sixteen cases of gonadal dysgenesis were included in this study: 5 with androgen insensitivity syndrome, 1 with 17-α-hydroxylase deficiency, 4 with true hermaphrodite, 2 with 45,X/46,XY gonadal dysgenesis, 1 with 45,X gonadal dysgenesis, 1 with XY pure gonadal dysgenesis, 1 with testicular regression, and 1 XY female who gave birth to a normal baby.

病例 对16例性腺发育不全患者：其中雄激素不敏感综合症5例、17α羟化酶缺乏症1例、真两性畸形4例、45，X性腺发育不全1例、XY单纯性腺发育不全1例、睾丸退化1例、血核型为46，XY但已分娩正常儿1例以及45，X/46，XY性腺发育不全2例。

Ectrodactyly, ectodermal dysplasia and clefting syndrome is characterized by split hand-split foot malformation, congenital ectodermal dysplasia and cleft lip with or without cleft palate.

目前，以先天性缺指、并指或手足裂和外胚叶发育不全伴或不伴腭裂的唇裂为主要临床表现的先天性缺指-外胚叶发育不全-唇/腭裂综合征的病因仍然不明，给疾病的防治带来了较大的困难。

An otherwise healthy 12-month-old girl presented for evaluation of reduced abduction of the left eye detected at 6 months of age. The remainder of the examination was unremarkable. A special MRI sequence-fast imaging employing steady-state acquisition-visualized the right but not the left sixth nerve cisternal segment. This is the first reported use of the MRI FIESTA sequence to diagnose aplasia of the sixth cranial nerve.

应用快速平衡稳态取像核磁技术检测第六颅神经发育不全：本研究首次报道利用 MRI FIESTA 诊断第六颅神经发育不全，一例12个月的婴儿其他各项指标正常，在6个月时发现左眼诱导注视减少，其他的检查未见明显异常，利用 MRI FIESTA 可检测到右侧第六颅神经，但左侧部分检测不到。

In this article, a case of cleidocranial dysplasia of a 25-year-old Taiwanese female is reported. She visited Taichung Veterans General Hospital Department of Dentistry for the treatment of dental caries in March, 2005. Her abnormalities were diagnosed by Oral and Maxillofacial Surgeon, and was later certified by physician of Genetic Consultation and radiologist.

本文报告一位25岁台湾女性颅锁骨发育不全病例於民国94年三月至台中荣总牙科部寻求龋齿诊治，经口腔颚面外科医师临床及影像检查后，初步臆断为颅锁骨发育不全症候群，后经遗传谘询及放射线部医师确定诊断为颅锁骨发育不良。

Fertile stamens 3, in a few flowers only anterior 2 fertile, posterior 1 depauperate or absent, often anterior 2 also depauperate; filaments densely white lanate; staminodes 3; antherodes 3-sect. Capsule ovoid, 1.5--1.7 cm, acute at apex.

能育雄蕊3，在数花内只前面的2枚能育，后面1发育不全或无，通常前面2也发育不全；花丝浓密的白色绵状毛；退化雄蕊3；退化花药 3全裂；蒴果卵球形，1.5-1.7厘米，锐尖的在先端。

Of the 19 cases,19 fetus were found,MRI confirmed 14 cases considered or suspected as fetal corpus callosum agenesis by US(8 cases are completed agenesis of corpus collosom-CACC,6 cases are partial agenesis of corpus collosom-PACC, and 5 cases had took on autopsy),however 3 cases are mild enlargement of lateral cerebral ventricle and 2 cases are leukodystrophy.In these cases,MRI confirmed a Dandy-Walker syndrome and a lipoma of corpus callosum suspected by US,detect a Dandy-Walker syndrome and a microcephalus made missed diagnoses by US.The fetal corpus callosum and additional cerebral anomalies were shown more clearly on MR T_2-weighted images.

胎儿胼胝体长度与额枕径的比值在24～36孕龄阶段相对较恒定。2、19例孕妇共检出胎儿19个，MRI证实超声疑诊的胎儿胼胝体发育不全14例(完全型胼胝体发育不全8例，部分型胼胝体发育不全6例，有胎儿尸检结果对照者5例)，3例为单纯侧脑室轻度扩张，2例考虑脑白质发育不良，合并Dandy—Walker综合征1例，胼胝体脂肪瘤1例，检出超声漏诊合并Dandy-Walker综合征1例及脑小畸形1例。

As she looked at Warrington's manly face, and dark, melancholy eyes, she had settled in her mind that he must have been the victim of an unhappy attachment.

每逢看到沃林顿那刚毅的脸，那乌黑、忧郁的眼睛，她便会相信，他一定作过不幸的爱情的受害者。

Maybe they'll disappear into a pothole.

也许他们将在壶穴里消失