Sharony R, Browne C, Lachman R S, Rimoin D L
Medical Genetics-Birth Defects Center, Cedars-Sinai Medical Center, Los Angeles, CA 90048.
Am J Obstet Gynecol. 1993 Sep;169(3):668-75. doi: 10.1016/0002-9378(93)90641-u.
We examined the accuracy of prenatal diagnosis of skeletal dysplasias and ways to refine this ability.
A total of 226 fetuses and stillbirths referred for suspected skeletal dysplasia were evaluated. The fetal age, mode of ascertainment, and referring diagnosis were analyzed with regard to the final diagnosis.
The leading mode of diagnosis was routine ultrasonography performed between 16 and 24 weeks' gestation. Twenty-two cases (9.7%) had previous sibs, parents, or cousins affected. The most common final diagnosis was osteogenesis imperfecta. In 15 cases (7%) the fetus did not appear to have a skeletal dysplasia or an obvious dysmorphic syndrome.
Prenatal diagnosis of skeletal dysplasia can be made as early as 14 weeks. Most cases are sporadic. Fetal radiographs help in reaching an accurate diagnosis or at least in identifying the probable lethal disorders.
我们研究了骨骼发育异常的产前诊断准确性以及提高该诊断能力的方法。
对总共226例因疑似骨骼发育异常而转诊的胎儿和死产儿进行了评估。针对最终诊断,分析了胎龄、确诊方式和转诊诊断情况。
主要诊断方式为在妊娠16至24周期间进行的常规超声检查。22例(9.7%)有患病的同胞、父母或表亲。最常见的最终诊断是成骨不全。15例(7%)胎儿似乎没有骨骼发育异常或明显的畸形综合征。
骨骼发育异常的产前诊断最早可在14周时做出。大多数病例为散发性。胎儿X线片有助于做出准确诊断,或至少有助于识别可能的致死性疾病。