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   osteogenesis imperfecta 在 生物学 分类中 的翻译结果: 查询用时:0.008秒
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osteogenesis imperfecta
相关语句
  成骨不全
    A pedigree investigation was carried out on 372 relatives in five generations of a proband of osteogenesis imperfecta. The results showed that there were 28 patients in the family. 10 of them died from other causes (5 adults and 5 children respectively).
    对成骨不全先证者上溯5代372人进行家系调查,发现该家系共有28例成骨不全,其中已死亡10例(成人、儿童各5例),均非死于本病;
短句来源
  成骨不全
    A pedigree investigation was carried out on 372 relatives in five generations of a proband of osteogenesis imperfecta. The results showed that there were 28 patients in the family. 10 of them died from other causes (5 adults and 5 children respectively).
    对成骨不全先证者上溯5代372人进行家系调查,发现该家系共有28例成骨不全,其中已死亡10例(成人、儿童各5例),均非死于本病;
短句来源
  “osteogenesis imperfecta”译为未确定词的双语例句
    A Report on 28 Cases in Five Generations in the Family of Autosomal Dominant Interifant Disease of Osteogenesis Imperfecta
    成骨不全显性遗传一家系五代28例报告
短句来源
  相似匹配句对
    A Report on 28 Cases in Five Generations in the Family of Autosomal Dominant Interifant Disease of Osteogenesis Imperfecta
    成骨不全显性遗传一家系五代28例报告
短句来源
    It could induce the osteogenesis reaction.
    同时生物接骨板在体内可诱导成骨反应
短句来源
    Regulatory Effect of IGFs Family on Osteogenesis
    IGFs家族对骨骼发育的调控机制研究
短句来源
    A pedigree investigation was carried out on 372 relatives in five generations of a proband of osteogenesis imperfecta. The results showed that there were 28 patients in the family. 10 of them died from other causes (5 adults and 5 children respectively).
    对成骨不全先证者上溯5代372人进行家系调查,发现该家系共有28例成骨不全,其中已死亡10例(成人、儿童各5例),均非死于本病;
短句来源
    DSPP Mutation in Dentinogenesis Imperfecta Shields Type Ⅱ and Mouse Model with Dspp Gene Mutation
    遗传性乳光牙本质致病基因的鉴定和Dspp基因敲除小鼠的建立
短句来源
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  osteogenesis imperfecta
Surgical treatment of the femur in osteogenesis imperfecta with intramedullary elongating rods
      
Beitrag zur Lehre von der Osteogenesis imperfecta tarda
      
Femurosteosynthesen mit dem Teleskopnagel nach Bailey-Dubow bei Osteogenesis imperfecta
      
Simultaneous Bilateral Tibial Tubercle Avulsion Fractures in a Boy with Osteogenesis Imperfecta
      
Treatment of children with osteogenesis imperfecta
      
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A pedigree investigation was carried out on 372 relatives in five generations of a proband of osteogenesis imperfecta. The results showed that there were 28 patients in the family. 10 of them died from other causes (5 adults and 5 children respectively). Other 18 cases are alive(12 adults and 6 children respectively). The height of the 28 cases were significantly lower than those of the same age. Furthermore, they all had blue scleras. Their clinical manifestations conformed to those of autosomal dominant...

A pedigree investigation was carried out on 372 relatives in five generations of a proband of osteogenesis imperfecta. The results showed that there were 28 patients in the family. 10 of them died from other causes (5 adults and 5 children respectively). Other 18 cases are alive(12 adults and 6 children respectively). The height of the 28 cases were significantly lower than those of the same age. Furthermore, they all had blue scleras. Their clinical manifestations conformed to those of autosomal dominant hereditary connective tissue disease. Among the living 18 cases, 6 suffered from deafness or hearing loss and 9 suffered from fracture (22 person-time altogether). According to the classification criteria in the literature, the clinical manifestations of the 28 cases conformed to those of type I and type Ⅲ. It is necessary to study further whether they belonged to the subtype between type I and type Ⅲ.

对成骨不全先证者上溯5代372人进行家系调查,发现该家系共有28例成骨不全,其中已死亡10例(成人、儿童各5例),均非死于本病;现生存18例(成人12例、儿童6例)。该28例均身材矮小、身高显著低于同龄正常者;均有蓝色巩膜;符合常染色体显性遗传缺陷的结缔组织病。现存活18例中,耳聋、听力下降6例;骨折9例(22例次),对照文献中分型标准,本组28例与Ⅰ型、Ⅲ型的部分临床特征相符,是否系介于Ⅰ型、Ⅲ型之间的亚型,有待于进一步研究。

 
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