Magnetic Resonance Imaging for Detection of Brain Abnormalities in Fetuses With Cleft Lip and/or Cleft Palate

被引:14
|
作者
Rosen, Heather [1 ,2 ]
Chiou, Grace J.
Stoler, Joan M. [3 ]
Mulliken, John B. [4 ]
Tarui, Tomo [5 ]
Meara, John G. [4 ]
Estroff, Judy A. [6 ,7 ]
机构
[1] Harvard Univ, Sch Med, Dept Plast & Oral Surg, Boston, MA USA
[2] Univ So Calif, Keck Sch Med, Dept Surg, Los Angeles, CA 90033 USA
[3] Childrens Hosp Boston, Dept Pediat, Div Genet, Boston, MA USA
[4] Childrens Hosp Boston, Dept Plast & Oral Surg, Boston, MA USA
[5] Childrens Hosp Boston, Dept Neurol, Boston, MA USA
[6] Childrens Hosp Boston, Dept Radiol, Boston, MA USA
[7] Childrens Hosp Boston, Adv Fetal Care Ctr, Boston, MA USA
来源
CLEFT PALATE-CRANIOFACIAL JOURNAL | 2011年 / 48卷 / 05期
关键词
anomalies; brain; cleft lip; cleft palate; fetal; magnetic resonance imaging; prenatal; COGNITIVE DYSFUNCTION; PRENATAL-DIAGNOSIS; ORAL CLEFTS; ADULT MALES; ANOMALIES; MALFORMATIONS;
D O I
10.1597/09-262
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective: To determine the prevalence of brain abnormalities identified by prenatal imaging of fetuses with cleft lip with or without cleft palate (CL/P) or cleft palate only (CP) and to compare with postnatal imaging and neurologic evaluation. Design: This was a retrospective review of radiologic images (magnetic resonance imaging [MRI] and sonography) of fetuses diagnosed with CL/P or CP at the Advanced Fetal Care Center at Children's Hospital Boston between 2002 and 2008. Images were reviewed for possible brain abnormalities by a pediatric radiologist who specializes in this field. Postnatal imaging was also assessed whenever available and correlated with clinical findings. Setting: A large, tertiary-care, academic pediatric hospital. Population: One hundred twenty-six fetuses and 105 corresponding infants. Results: Brain abnormalities were found in 8 of 126 fetuses (6.3%) by prenatal MRI. The malformations were corpus callosal dysgenesis (n = 3), encephalocele (n = 1), hypoplasia of the cerebellar hemispheres or vermis (n = 3), and white matter neuronal migration anomaly (n = 1). An additional 2 patients were diagnosed with brain abnormalities postnatally that had not been detected on prenatal imaging. Conclusions: The possibility of brain anomalies should be assessed in a fetus found to have CL/P or CP by sonography and/or MRI. Central nervous system imaging and careful neurodevelopmental follow-up is indicated in these infants.
引用
收藏
页码:619 / 622
页数:4
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