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骨骼发育不良的胎儿生物测量:一项多中心研究。

Fetal biometry of skeletal dysplasias: a multicentric study.

作者信息

Goncalves L, Jeanty P

机构信息

Department of Radiology and Radiological Sciences, Vanderbilt University, Nashville, TN 37232-5316.

出版信息

J Ultrasound Med. 1994 Dec;13(12):977-85. doi: 10.7863/jum.1994.13.12.977.

Abstract

Twenty-three diagnostic centers worldwide contributed 127 cases of 17 skeletal dysplasias. Discriminant analysis showed that the femur length was the best biometric parameter to distinguish among the five most common disorders in this series (thanatophoric dysplasia, osteogenesis imperfecta type II, achondrogenesis, achondroplasia and hypochondroplasia). Fifty-four percent of fetuses with femur length below 30% of the mean for gestational age had achondrogenesis. Seventy-eight percent of measurements between 40 and 60% of the mean for gestational age represented either thanatophoric dysplasia or osteogenesis imperfecta type II. Fetuses who had over 80% of the mean for gestational age had predominantly hypochondroplasia, achondroplasia, and osteogenesis imperfecta type III.

摘要

全球23个诊断中心提供了17种骨骼发育不良的127个病例。判别分析表明,股骨长度是区分该系列中五种最常见疾病(致死性骨发育不良、II型成骨不全、软骨发育不全、软骨发育不良和低软骨发育不良)的最佳生物测量参数。股骨长度低于孕周均值30%的胎儿中,54%患有软骨发育不全。孕周均值40%至60%之间的测量值中,78%代表致死性骨发育不良或II型成骨不全。孕周均值超过80%的胎儿主要患有低软骨发育不良、软骨发育不良和III型成骨不全。

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