Syndromic micrognathia and peri-natal management with the ex-utero intra-partum treatment (EXIT) procedure

被引:10
作者
Costello, B. J. [1 ,2 ]
Hueser, T. [1 ]
Mandell, D. [3 ]
Hackam, D. [4 ,5 ]
Prosen, T. L. [6 ]
机构
[1] Univ Pittsburgh, Sch Dent Med, Dept Oral & Maxillofacial Surg, Pittsburgh, PA 15260 USA
[2] Childrens Hosp Pittsburgh, Div Pediat Oral & Maxillofacial Surg, Pittsburgh, PA USA
[3] Ctr Pediat ENT Head & Neck Surg, Boynton Beach, FL USA
[4] Childrens Hosp Pittsburgh, Dept Surg, Div Pediat Surg, Pittsburgh, PA USA
[5] Univ Pittsburgh, Sch Med, Pittsburgh, PA 15260 USA
[6] Univ Minnesota, Med Ctr, Dept Obstet Gynecol & Womens Hlth, Div Maternal Fetal Med, Minneapolis, MN 55455 USA
关键词
prenatal; cleft; craniofacial; fetus; maternal-fetal medicine; EXIT procedure;
D O I
10.1016/j.ijom.2010.02.017
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Many advances in healthcare are built on advances in technology. In the case of fetal medicine, technology has availed an entirely new patient population. The authors report a case of severe micrognathia and Pierre Robin Sequence that was diagnosed prenatally. Antenatal planning and treatment were instituted via the Fetal Diagnosis/Treatment Team to avoid loss of the neonate's airway. An EXIT procedure was utilized to ensure a secure airway. The benefits of team care for these types of deformities are highlighted including the importance of craniomaxillofacial specialists.
引用
收藏
页码:725 / 728
页数:4
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