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13 - Antenatal diagnosis of selected defects

Published online by Cambridge University Press:  05 March 2012

Michael A. Posencheg
Affiliation:
University of Pennsylvania
Eileen Y. Wang
Affiliation:
University of Pennsylvania
Haresh Kirpalani
Affiliation:
Children's Hospital of Philadelphia
Monica Epelman
Affiliation:
Children's Hospital of Philadelphia
John Richard Mernagh
Affiliation:
McMaster University, Ontario
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Publisher: Cambridge University Press
Print publication year: 2011

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References

N. S., Adzick, E. A., Thom, C. Y., Spong, et al. A randomized trial of prenatal versus postnatal repair of myelomeningocele. N Engl J Med 2011; 364(11):993–1004.Google Scholar
B. R., Benacerraf, T. D., Shipp, B., Bromley, D., Levine. What does magnetic resonance imaging add to the prenatal sonographic diagnosis of ventriculomegaly?J Ultrasound Med 2007; 26(11):1513–22.Google Scholar
D., Cafici, W., Sepulveda. First-trimester echogenic amniotic fluid in the acrania-anencephaly sequence. J Ultrasound Med 2003; 22(10):1075–9.Google Scholar
J. E., Corteville, J. M., Dicke, J. P., Crane. Fetal pyelectasis and Down syndrome: is genetic amniocentesis warranted?Obstet Gynecol 1992; 79(5 Pt. 1):770–2.Google Scholar
S. D., Grosse, J. S., Collins. Folic acid supplementation and neural tube defect recurrence prevention. Birth Defects Res A Clin Mol Teratol 2007; 79(11):737–42.Google Scholar
D. S., Hains, C. M., Bates, S., Ingraham, A. L., Schwaderer. Management and etiology of the unilateral multicystic dysplastic kidney: a review. Pediatr Nephrol 2009; 24(2):233–41.Google Scholar
H. L., Hedrick. Management of the prenatally diagnosed congenital diaphragmatic hernia. Semin Fetal Neonatal Med 2010; 15:21–7.Google Scholar
A. M., Ierullo, R., Ganapathy, S., Crowley, et al. Neonatal outcome of antenatally diagnosed congenital cystic adenomatoid malformations. Ultrasound Obstet Gynecol 2005; 26(2):150–3.Google Scholar
D. D., Johnson, D. H., Pretorius, N. E., Budorick, et al. Fetal lip and primary palate: threedimensional versus two-dimensional US. Radiology 2000; 217(1):236–9.Google Scholar
P. N., Jone, K. O., Schowengerdt. Prenatal diagnosis of congenital heart disease. Pediatr Clin N Am 2009; 56:709–15.Google Scholar
D. M., Kitchens, C. D. A., Herndon. Antenatal hydronephrosis. Curr Urol Rep 2009; 10:126–33.Google Scholar
D., Krakow, R. S., Lachman, D. L., Rimoin. Guidelines for the prenatal diagnosis of fetal skeletal dysplasias. Genet Med 2009; 11(2):127–33.Google Scholar
P., Laje, K. W., Leichty. Postnatal management and outcome of prenatally diagnosed lung lesions. Prenat Diagn 2008; 28:612–18.Google Scholar
D. J., Ledbetter. Gastroschisis and omphalocele. Surg Clin North Am 2006; 86(2):249–60.Google Scholar
D., Lewis, J. E., Tolosa, M., Kaufmann, et al. Elective cesarean delivery and long-term motor function or ambulation status in infants with meningomyelocele. Obstet Gynecol 2004; 103(3):469–73.Google Scholar
D. A., Luthy, T., Wardinsky, D. B., Shurtleff, et al. Cesarean section before the onset of labor and subsequent motor function in infants with meningomyelocele diagnosed antenatally. N Engl J Med 1991; 324(10):662–6.Google Scholar
S., Mercier, C., Dubourg, M., Belleguic, et al. Genetic counseling and “molecular” prenatal diagnosis of holoprosencephaly (HPE). Am J Med Genet C Semin Med Genet 2010; 154C(1):191–6.Google Scholar
G., Sidhu, J., Beyene, N. D., Rosenblum. Outcome of isolated antenatal hydronephrosis: a systematic review and meta-analysis. Pediatr Nephrol 2006; 21(2):218–24.Google Scholar

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