畸形的

Istal arthrogryposis type 2B,one of most common types of DAs,is a multiple congenital contracture disorder characterized by contractures of the distal joints of limbs without neurological and skeletal muscle defect.

A2B是一种先天性遗传病，主要表现为2个或2个以上关节的挛缩畸形，并且不包括由神经和肌肉病变所导致的关节畸形。

Results The long term results of the vascularized fibular graft varied in different types of bone defects. Nine patients with congenital pseudoarthrosis of tibia had the limb function restored in 65％ and one had nonunion of fibular graft, 3 fractures(7 times), and 5 angular deformities. Three patients with congenital radial deficiency had 62％ restoration of the limb function. All of them showed early closure of epiphyses of the grafted fibulae. Five cases with osteomyelitis and bone defects combined soft tissue deficiency had 94％ restoration of the limb function, and only one occurred fracture of fibular graft. One case with soft tissue defect and concomitant ulnar defect, ulnar nerve and median nerve injury, 67％ function of limb was recovered, and union of fibula graft was good. 100％ function of limb was recovered in 1 case with cavernoma of radius and without occurring valgus deformity of donor site.

结果应用带血管腓骨移植修复骨缺损的远期效果因缺损类型的不同而存在较大差异。9例先天性胫骨假关节患者，术后肢体功能恢复65％，其中移植腓骨骨不连1例、骨折3例(7次)、成角畸形5例；3例先天性桡骨缺如患者，术后肢体功能恢复62％，3例术后均出现移植腓骨骨骺线早闭，畸形复发；5例骨髓炎、骨外露、骨缺损并软组织缺损患者，术后肢体功能恢复94％，仅1例发生移植腓骨骨折；1例前臂软组织缺损并尺骨缺损，尺神经、正中神经损伤者，术后肢体功能恢复67％，骨愈合顺利；1例桡骨海绵状血管瘤者，术后肢体功能恢复100％，骨愈合顺利。

As a plastic surgery of aedea, penis lengthening surgery is performed to rectify the short-penis abnormality、 increase the length and resume its normal function mainly for those people with inborn short-penis abnormality and those with scar contracture and coloboma after all kinds of trauma、 burn of penis.

阴茎延长术是一种外生殖器整形手术，主要针对先天性阴茎短小畸形及各种创伤、烧伤后的阴茎瘢痕挛缩、缺损患者，旨在矫正阴茎短小畸形、延长阴茎、恢复正常功能；同时对于正常人群，此方法也能达到改善外观及功能的作用。

Based the above research, we chosen 48 cephalometric radiographs of skeletal classⅢocclusion (18-39 years old, ANB4°) and measured with computer assistant Delaire cephalometric analysis. The data were deal with ANOVA analysis through SAS9.0 statistical software. The research divided the cranio-maxillo-facial hard tissue structure feature of skeletal classⅢinto four classifications through Delaire cephalometric analysis including hypo-divergent, hyper-divergent, maxilla normal and glenoid fossa retrocession, nine parameters of four groups have significantly variability through ANOVA analysis(P.05),for example, anterior cranial base angle, sphenoidal angle, percentage of craniospinal area to cranial depth ,percentage of craniofacial area to cranial depth and so on.

在上述研究的基础上，首先选取48例骨性Ⅲ类错牙合畸形患者(18-39岁，ANB角4°)应用Delaire头影测量分析法进行测量，经SAS9.0行ANOVA分析，将骨性Ⅲ类错牙合畸形区分为低角型、高角型、上颌正常型和关节窝后移型四组，四组均数ANOVA分析发现九项分析指标的均数差异均有统计学意义(P.05)，如蝶鞍角、前颅基底角、颅面区比和颅颈区比。

Result: the reasons of hand burn scar contracture in 74 cases included deepened infection due to inappropriate treating the wound surface in the early stage, the form of hyperplastic scar due to failing to accept the dermoplasty in deep ii burn and late operation or thin free skin graft in deep burn and inadequate rehabilitation exercise after operation.

结果：74例手烧伤后瘢痕挛缩畸形产生的主要原因为：①创面早期处理不当致感染加深；②深II度烧伤病人不接受植皮而形成增生性瘢痕；③深度烧。。。本文由网友上传，与本网无关摘要：探讨手部烧伤后瘢痕挛缩畸形较为有效的防治方法。

Using the following methods to treat one patient of congenital absence of the tibia with fork-shaped lower femur, the caput fibulae forming unstable knee joint, and concomitant knee flexion 95 degree.

方法1例先天性右胫骨完全缺如，股骨下端呈叉状，腓骨头与股骨下端形成不稳定的膝关节，伴屈膝畸形95 ，于1岁半实施股骨下端修整术，5岁和8岁时分两期安装Ilizarov膝关节牵伸器，牵拉矫正屈膝畸形达到伸膝0 位，使腓骨头与股骨下端成膝关节，拆牵伸器后装配能稳定膝关节的下肢补高矫形器行走。

Background and Objective: Cerebral Arteriovenous malformation is the most familiar cerebrovascular malformation. The clinical manifestations contain hemorrhage, refractory headache, and epilepsy etc, part of the patients show progressive hemiparalysis due to long-term intracephalic steal blood.

背景和目的：脑动静脉畸形(arteriovenous malformation， AVM)为最常见的脑血管畸形，临床表现为出血、顽固性头痛、癫痫等；部分患者因长期脑内盗血而进行性偏瘫，严重威胁人们的生存质量和生命安全。

The results showed that all of them could detect the presence of ZFY DNA sequences except a 46 XX"male"and a 46 XX hermaphrodite, our findings confirmed that Ferguson-Smith〔1966〕 forwarded the hypothesis that the X-Y intercharge model for XX maleness can be regarded as an abnormal exchange initaited in a region proximal to TDF and extending to the telomere,and,also strongly suggested that ZFY gene palyed an important role in sex determining of human.

结果除一例46XX两性畸形，一例46XX&男性&外，余均能检测到ZFY DNA序列(ZFY DNA序列存在于46XX真两性畸形和45XO Turner's综合症，在国内外尚未见报道)。证实了1966年，Ferguson-Smith提出的理论：在父源减数分裂期间，X-Y发生不等交换，导致Y染色体DNA插入性易位。XX男性是由于Y染色体上的TDF基因转移至X染色体上所致。

Objective Analysis inherit and environmental factors of the 43 collected microtia cases, sequence GSC gene and investigate the reason of congenital microtia.

目的 对收集的43例先天性小耳畸形患者进行遗传及环境因素分析，并对GSC基因测序，探讨先天性小耳畸形发生的原因。

The typi ca1 symptom j s fold and b1 istering, even d istortj on, 1ops i ded j -- eaf, shorti ng p ant, there are motley with 1ight green and deep green, and some of the motey are ye1wt MM 1eave M tny: the i.1--1ed has arias mosai c, 1ops i ded, and the tissue of the i11--1eaf has deteriorated exceeding1y, with s1ender pteridophyte 1.eaves, i l1 p1ant is green--yeI 1ow, obvious1y shortened in joint, the who1e p1ant serious1y shortened and grows thickly.

南瓜病毒病的典型症状为皱缩有疱斑、甚至扭曲，病叶畸形，植株矮化；花叶叶片上出现淡绿色和深绿色相间的斑驳，有的斑驳明显黄化；蕨叶丛枝型：病叶不但严重花叶、畸形，而且叶肉组织极度退化，纤细呈蕨叫叶状，病株黄绿色，节间明显缩短，整个植株严重矮化丛枝状。

I am accused of being overreligious," she said in her quiet, frank manner,"but that does not prevent me thinking the children very cruel who obstinately commit such suicide.""

客人们在卡罗利娜·埃凯家里，举止就文雅一些，因为卡罗利娜的母亲治家很严厉。

Designed by French fashion house Herm è s, this elegant uniform was manufactured in our home, Hong Kong, and was the first without a hat.

由著名品牌 Herm è s 设计，这件高贵的制服是香港本土制造，是我们第一套不配帽子的制服。