VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer

Objective: We present a case of VACTERL association with hydrocephalus (VACTERL-H) in a fetus conceived by in vitro fertilization (IVF) and embryo transfer (ET) and review the literature. Case report: A 35-year-old woman presented with multiple fetal anomalies at 22 weeks of gestation. She and her h...

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Main Authors: Chih-Ping Chen, Tung-Yao Chang, Yi-Yung Chen, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
Format: Article
Language:English
Published: Elsevier 2013-12-01
Series:Taiwanese Journal of Obstetrics & Gynecology
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S102845591300185X
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spelling doaj-d7a416ecf0c74079b6b9971dbe00df6d2020-11-24T23:05:57ZengElsevierTaiwanese Journal of Obstetrics & Gynecology1028-45592013-12-0152457557910.1016/j.tjog.2013.10.022VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transferChih-Ping Chen0Tung-Yao Chang1Yi-Yung Chen2Schu-Rern Chern3Jun-Wei Su4Wayseen Wang5Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, TaiwanTaiji Fetal Medicine Center, Taipei, TaiwanDepartment of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, TaiwanDepartment of Medical Research, Mackay Memorial Hospital, Taipei, TaiwanDepartment of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, TaiwanDepartment of Medical Research, Mackay Memorial Hospital, Taipei, TaiwanObjective: We present a case of VACTERL association with hydrocephalus (VACTERL-H) in a fetus conceived by in vitro fertilization (IVF) and embryo transfer (ET) and review the literature. Case report: A 35-year-old woman presented with multiple fetal anomalies at 22 weeks of gestation. She and her husband were non-consanguineous and there was no family history of congenital malformations. This was her second pregnancy conceived via IVF-ET. Two embryos had been implanted and only one survived. She underwent chorionic villus sampling at 17 weeks of gestation because of oligohydramnios and advanced maternal age. Cytogenetic analysis revealed a karyotype of 46,XY, and array comparative genomic hybridization analysis revealed no genomic imbalance. Prenatal ultrasound at 21 weeks of gestation revealed a singleton with fetal biometry equivalent to 18 weeks, ventriculomegaly, a small cerebellum, and a ventricular septal defect. Level II ultrasound showed a single umbilical artery, scoliosis, a right club hand, radial aplasia, and renal agenesis. The parents elected to terminate the pregnancy at 22 weeks of gestation, and a fetus was delivered with bilateral arthrogryposis, right radial aplasia, a club hand and thumb aplasia, hypoplasia of the left thumb, scoliosis, and an imperforate anus. The clinical findings were consistent with the diagnosis of VACTERL-H. Molecular analysis of PTEN, FANCB, and HOXD13 genes revealed no mutation. Conclusion: Prenatal diagnosis of radial ray defects in fetuses conceived by assisted reproductive technology should include a differential diagnosis of VACTERL association with anorectal malformation. VACTERL-H may occur in pregnancy after IVF-ET.http://www.sciencedirect.com/science/article/pii/S102845591300185Xassisted reproductive technologyhydrocephalusin vitro fertilizationprenatal diagnosisVACTERL association
collection DOAJ
language English
format Article
sources DOAJ
author Chih-Ping Chen
Tung-Yao Chang
Yi-Yung Chen
Schu-Rern Chern
Jun-Wei Su
Wayseen Wang
spellingShingle Chih-Ping Chen
Tung-Yao Chang
Yi-Yung Chen
Schu-Rern Chern
Jun-Wei Su
Wayseen Wang
VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer
Taiwanese Journal of Obstetrics & Gynecology
assisted reproductive technology
hydrocephalus
in vitro fertilization
prenatal diagnosis
VACTERL association
author_facet Chih-Ping Chen
Tung-Yao Chang
Yi-Yung Chen
Schu-Rern Chern
Jun-Wei Su
Wayseen Wang
author_sort Chih-Ping Chen
title VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer
title_short VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer
title_full VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer
title_fullStr VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer
title_full_unstemmed VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer
title_sort vacterl association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer
publisher Elsevier
series Taiwanese Journal of Obstetrics & Gynecology
issn 1028-4559
publishDate 2013-12-01
description Objective: We present a case of VACTERL association with hydrocephalus (VACTERL-H) in a fetus conceived by in vitro fertilization (IVF) and embryo transfer (ET) and review the literature. Case report: A 35-year-old woman presented with multiple fetal anomalies at 22 weeks of gestation. She and her husband were non-consanguineous and there was no family history of congenital malformations. This was her second pregnancy conceived via IVF-ET. Two embryos had been implanted and only one survived. She underwent chorionic villus sampling at 17 weeks of gestation because of oligohydramnios and advanced maternal age. Cytogenetic analysis revealed a karyotype of 46,XY, and array comparative genomic hybridization analysis revealed no genomic imbalance. Prenatal ultrasound at 21 weeks of gestation revealed a singleton with fetal biometry equivalent to 18 weeks, ventriculomegaly, a small cerebellum, and a ventricular septal defect. Level II ultrasound showed a single umbilical artery, scoliosis, a right club hand, radial aplasia, and renal agenesis. The parents elected to terminate the pregnancy at 22 weeks of gestation, and a fetus was delivered with bilateral arthrogryposis, right radial aplasia, a club hand and thumb aplasia, hypoplasia of the left thumb, scoliosis, and an imperforate anus. The clinical findings were consistent with the diagnosis of VACTERL-H. Molecular analysis of PTEN, FANCB, and HOXD13 genes revealed no mutation. Conclusion: Prenatal diagnosis of radial ray defects in fetuses conceived by assisted reproductive technology should include a differential diagnosis of VACTERL association with anorectal malformation. VACTERL-H may occur in pregnancy after IVF-ET.
topic assisted reproductive technology
hydrocephalus
in vitro fertilization
prenatal diagnosis
VACTERL association
url http://www.sciencedirect.com/science/article/pii/S102845591300185X
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