Twenty - five cases of achondroplasia followed for a period of recent three years are reviewed 摘要我们分析在3年中遇到的25例软骨发育不全侏儒。
2.
Genetic counselling and the management of complications in achondroplasia are important 对于软骨发育不全侏儒患者的遗传谘询以及其并发症的处理是很重要的。
3.
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
4.
The head girths of several patients were above the 97th percentile of the normal growth curve , but were normal in a special growth chart for achondroplasia 有几位患者的头围大于正常生长曲线的第97个百分位数，可是在软骨发育不全侏儒患者特有的生长曲线中，这些头围是正常的。
5.
Dr chahira kozma , of georgetown university hospital , washington , has used inscriptions and representations on tomb and temple walls , papyrus documents and other objects , as well as human remains , to see how achondroplasia , a cause of the most common type of dwarfism , was regarded in ancient times 据每日电讯12月28日报道，通过对古代的铭神殿文献资料和古人类遗骸的研究，美国华盛顿州乔治敦大学医院的科兹马博士指出，侏儒们在古埃及社会受到尊重，享有较高的社会地位。
