发育异常

We discuss a series of 11 patients seen at the Cole Eye Institute with the condition of myelinated retinal nerve fibers, myopia, and amblyopia and describe the clinical characteristics.

我们讨论了 Cole 眼科中心11例视网膜有髓神经纤维，近视和弱视的病人的临床特征。3名病人已经有视神经发育异常，并对相关文献进行了综述。

Lipid peroxidation would cause the deficiency of myelinogenesis, Dysfunction of synaptic conduction and developmental anomaly of nerve cell if the deficiency of completely.

当硒缺乏时，硒蛋白活性降低，清除H2O2能力减弱，脂质过氧化导致髓鞘形成不良，突触传导障碍，神经元发育异常，造成严重的脑功能紊乱。

Recently, the gene responsible for nevoid basal cell carcinoma syndrome, an autosomal dominant disorder characterized by multiple malformations and susceptibility to a variety of tumors and, particularly, to BCC, has recently been identified as PTCH.

痣样基底细胞癌症候群是一种体染色体显性遗传疾病，其主要表现有基底细胞癌、成齿的角质囊肿和其他多种骨骼发育异常，这个疾病被认为和PTCH基因突变有关。

Stone fruit trees can not set fruits when abnormal germ development occurs; while pomaceous fruit trees can set fruits without seeds, but the pulp cells grow very slow.

核果类果树在胚芽发育异常时不能坐果。仁果类果树在没有种子时可以坐果，但果肉细胞生长缓慢。

Stone fruit trees can not set fruits when abnormal germ development occurs; while pomaceous fruit trees can set fruits without seeds, but the pulp cells grow very slow.

种子产生的激素影响坐果、果实生长和植株体内激素平衡。核果类果树在胚芽发育异常时不能坐果。

We studied the mutation of PDS gene in children diagnosed to have prelingual non-syndromic hearing loss with concomitant bilateral large vestibular aqueduct and Mondini's dysplasia. We tried to find the correlation between non-syndromic hearing loss in local patients and PDS gene, and to establish the basic data of PDS gene mutations in Taiwan.

本篇研究之目的，乃对於患有非症候群学语前听障并合并双侧大前庭导水管及Mondini氏发育异常（Mondini's dysplasia）的儿童，作基因的分析，尝试找出本土非症候群听障与PDS基因的关连性，以建立台湾地区PDS基因突变的基本资料。

Paraffin slides observation found that the microspore of the RNMS line failed to vacuolate after its morphogenesis, disassembled and disappeared at last. After microspore morphogenesis, the breaking down of tapetum cells was delayed until microspore breading down.

石蜡切片细胞学观察，发现该隐性核不育能形成正常的四分体孢子，四分体释放出小孢子后，在单核花粉进入液泡化时小孢子的发育异常，不进行正常的液泡化，逐渐开始解体和消失；相应的绒毡层在小孢子形成后的降解延迟，绒毡层细胞的体积略有增大，在小孢子降解快结束时也很快解体。

Objective:To explore the clinical and pathological dignosis of fibrous dysplasia of bone and ossifying fibroma for improving the dignsis accuracy.

骨纤维结构不良、骨化性纤维瘤两种病的发病部位和组织结构均有相似之处，前者属骨发育异常瘤样病变 [1] 。

Drugs, many of our medicines, including the Anti-allergy element anticoagulant drugs can all be affected, there are special immune agents, antibiotics, anti-immune drugs, analgesics can result in the child cardiac abnormalities, and this is The most common number of factors.

药物，我们很多药物，包括抗敏素、抗凝的药物等都可以影响，还有特殊的免疫制剂、抗菌药物、抗免疫的药物、镇痛药都可以造成孩子心脏发育异常，这就是最常见的几个因素。

This condition is characterized by severe skeletal and dental malformations and underdevelopment, including partial or total absence of unilateral or bilateral clavicles, multiple impacted supernumerary teeth and impacted permanent teeth.

临床表徵多呈现严重骨骼及齿列发育异常，包括单侧或双侧锁骨部分或全部缺失、多发性阻生齿及赘生齿等。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。