发育不良

The following databases have been developed and are maintained by the OFA today: Hip Dysplasia, Elbow Dysplasia, Patellar Luxation, Autoimmune Thyroiditis, Congenital Cardiac Disease, Sebaceous Adenitis, Congenital Deafness, and others.

今天OFA主要发展的领域有，髋关节发育不良，肘关节发育不良，膝关节脱臼，自我免疫性甲状腺炎，先天性心脏病，脂肪性腺炎，先天性耳聋等。

Uni- or bilateral radial ray malformation including thenar hypoplasia, thumb hypoplasia/aplasia, triphalangeal, preaxial polydactyly, clubhand, deviation of the forearms, Duane anomaly, sensorineural or conductive deafness, and renal abnormalities

单侧或双侧桡骨线变形包括手掌发育不良，拇指发育不良/发育不全，三指节畸形，轴前并指畸形，畸形手，前臂偏斜，Duane异常，感觉神经性或传导性耳聋，和肾的异常。

It may be because the external ear dysplasia caused by hearing impairment, such as cochlear dysplasia, are curable by surgery; if it is caused by nerve connection, you need not worry too much pessimism and 宝宝 are still very small, in the infancy of the metabolic capacity of a strong , has many defects can be improved through its own, this is Doctor allows you to review the causes of each month.

它可能会因为外耳发育不良引起的听力障碍，比如耳蜗发育不良，是可以通过手术治愈的；如果是神经方面引起的，您也不用太悲观，宝宝还小，在婴儿时期的代谢能力很强，有很多缺陷都是可以通过自身完善的，这也是医生让您每月复查的原因。

The deficiency kidney-yang syndrome and dysplasia of uterus in rats were established by injecting hexadecadrol and bilateral oophorectomy.

观察毓官胶囊对肾阳虚型子宫发育不良大鼠IL2（自介素-2）-IFN-NKC免疫调节网的影响，探讨其治疗子宫发育不良的机制。

Hip dysplasia, osteochondritis and elbow dysplasia are certainly possible.

髋关节发育不良，骨软骨炎和肘部发育不良有一定可能的。

Microcephaly, occipital meningocele, dysplastic ears, optic atrophy, vertebral abnormalities, limb problems including radiohumeral synostosis, subluxation of one hip, joint contractures, and focal femoral hypoplasia.

小头畸形，枕部脑脊髓膜膨出，耳发育不良，视神经萎缩，脊椎异常，四肢问题包括：桡肱骨结合、一侧髋关节脱位、关节挛缩和灶性股骨发育不良。

Other major features include: partial or complete callosal agenesis, cortical malformations periventricular and subcortical heterotopias, cysts around the 3rd ventricle and/or choroid plexuses, papillomas of choroid plexuses, hypoplastic cerebellum, retrobulbar cysts, microophthalmia and colobomas.

其他主要表现包括：部分或完全的胼胝体发育不良，皮质畸形，脑室周，皮质下异位，环绕三脑室和脉络丛囊肿，脉络丛乳头状瘤，小脑发育不良，眼球后囊肿

The corpus callosum is not isible in the standard transerse iews of the brain but agenesis of the corpus callosum may be suspected by the absence of the caum septum pellucidum and the 'teardrop' configuration of the lateral entricles (enlargement of the posterior horns).

诊断：正常在脑的标准横切面上看不到胼胝体，通常通过透明隔腔小时和侧脑室的泪滴状改变怀疑有胼胝体的发育不良，确诊胼胝体发育不良需要在正中冠状面和正中矢状面上，一般需要做阴道B超显示。

Paper 2:Mutation analysis of EDA gene in Chinese families with X-linked hypohidrotic ectodermal dysplasiaX-linked hypohidrotic ectodermal dysplasia(XLHED,MIM305100) is a recessive disease characterized by severe hypohidrosis,hypotrichosis and hypodontia.

论文二X连锁无汗/少汗型外胚层发育不良中EDA基因致病突变鉴定X连锁隐性无汗/少汗型外胚层发育不良(X-linked anhidrotic/hypohidroticectodermal dysplasia，XLHED；MIM305100)是无汗/少汗型外胚层发育不良(anhidrotic/hypohidrotic ectodermal dysplasia，EDA)中最常见的一种，约占95%。

Experimental results show that there are existing some indifferent mechanisms to the pollen sterilization of the Ms types: during the period of single nucleic to three nucleic pollen cell,we observed that the cell of xylem and phloem in anther septum abnormally developed,also the cell in the sheath of vascular bundle,smaller and arranged irregularly; the metabolic block developed too,es...

结果表明，不育类型的花粉败育有着一些共同的机理：在花粉单核期至三核期可见到花药隔维管束的木质部及韧皮部细胞发育较差，维管束鞘细胞发育不良，体积较小，排列紊乱；在单核花粉期至三核花粉期均发生物质代谢障碍，特别在花药部位尤为明显；由于维管束发育不良和花药物质代谢障碍，导致了花粉缺乏营养而败育。

On closer examination, though, this is not a vote for multilateralism but just the opposite.

仔细审视后我们发现，这并非是对多边主义投出的赞成票，而是恰好相反。

Uncovering their weak spots, so I can defeat them.

揭露出他们的弱点，这样我就可以打败他们了。