医学
产前诊断
妊娠期
伯特症候群
胎儿
产科
怀孕
超声波
小脑蚓部
羊水过少
心室肥大
放射科
小脑
内科学
纤毛
细胞生物学
生物
遗传学
作者
Dan Doherty,Ian A. Glass,Joseph R. Siebert,Peter J. Strouse,Melissa A. Parisi,Dennis Shaw,Phillip F. Chance,Mason Barr,David A. Nyberg
摘要
OBJECTIVES: To describe the prenatal imaging findings in fetuses at risk for Joubert syndrome (JS), review the literature and propose a protocol for prenatal diagnosis of JS using ultrasound and MRI. METHODS: We reviewed prenatal ultrasound and fetal MRI studies in two pregnancies at 25% recurrence risk for JS and correlated these findings with gross neuropathology in one affected fetus. RESULTS: While abnormalities such as occipital encephalocele or enlarged cisterna magna have been identified before mid-trimester, the definitive diagnosis of JS, based on core cerebellar findings, has only been possible after 17 weeks' gestation. CONCLUSIONS: With longitudinal monitoring, it is possible to diagnose JS in at-risk pregnancies before 24 weeks' gestation. On the basis of our data and review of the literature, we propose a protocol for monitoring pregnancies at risk for JS, utilizing serial ultrasounds combined with fetal MRI at 20-22 weeks' gestation to maximize the accuracy of prenatal diagnosis.
科研通智能强力驱动
Strongly Powered by AbleSci AI