Cover Image

Detection of paternal origin of fetal trisomy 18 in a pregnancy conceived by assisted reproductive technology and in vitro fertilization

Objective: We present detection of paternal origin of fetal trisomy 18 in a pregnancy conceived by assisted reproductive technology (ART) and in vitro fertilization (IVF). Case report: A 39-year-old woman underwent ART and IVF because of primary infertility. The woman was infertile because of myoma...

Full description

Saved in:

Bibliographic Details
Main Authors:	Chih-Ping Chen (Author), Schu-Rern Chern (Author), Liang-Kai Wang (Author), Shin-Wen Chen (Author), Fang-Tzu Wu (Author), Dai-Dyi Town (Author), Wayseen Wang (Author)
Format:	Book
Published:	Elsevier, 2020-07-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

Monozygotic twins with trisomy 18 of paternal origin: prenatal diagnosis and molecular cytogenetic characterization in a pregnancy with one structurally abnormal living fetus and one intrauterine fetal demise
by: Chih-Ping Chen, et al.
Published: (2012)

Detection of paternal origin of fetal trisomy 21 in a pregnancy with isolated ventriculomegaly but without advanced parental age
by: Chih-Ping Chen, et al.
Published: (2020)

Prenatal diagnosis of maternal uniparental disomy 5 by amniocentesis associated with confined placental mosaicism for trisomy 5 and fetal trisomy 21 in a pregnancy
by: Chih-Ping Chen, et al.
Published: (2020)

Detection of placental mosaic trisomy 17 in a pregnancy associated with mosaicism for trisomy 17 in a single colony at amniocentesis with a favorable outcome
by: Chih-Ping Chen, et al.
Published: (2021)

Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results
by: Chih-Ping Chen, et al.
Published: (2020)

Prenatal diagnosis and molecular genetic analysis of recurrent trisomy 18 of maternal origin in two consecutive pregnancies
by: Chih-Ping Chen, et al.
Published: (2023)

Prenatal diagnosis of mosaicism for trisomy 7 in a single colony at amniocentesis in a pregnancy with a favorable outcome
by: Chih-Ping Chen, et al.
Published: (2019)

Mosaic trisomy 22 at amniocentesis: Prenatal diagnosis and literature review
by: Chih-Ping Chen, et al.
Published: (2019)

Prenatal diagnosis of trisomy 11 in a single colony of cultured amniocytes at amniocentesis in a pregnancy with a favorable outcome
by: Chih-Ping Chen, et al.
Published: (2021)

Mosaic trisomy 14 at amniocentesis: Prenatal diagnosis and literature review
by: Chih-Ping Chen, et al.
Published: (2013)

VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer
by: Chih-Ping Chen, et al.
Published: (2013)

First-trimester diagnosis of recurrent omphalocele associated with fetal trisomy 18 but without parental mosaicism
by: Chih-Ping Chen, et al.
Published: (2015)

Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma
by: Chih-Ping Chen, et al.
Published: (2015)

Concordant myelomeningocele in dizygotic twins conceived by intracytoplasmic sperm injection, in vitro fertilization, and embryo transfer
by: Chih-Ping Chen, et al.
Published: (2013)

Concomitant Omphalocele and Anencephaly Associated with Trisomy 18 and Arthrogryposis Diagnosed in Early Pregnancy
by: Chih-Ping Chen, et al.
Published: (2008)

Prenatal diagnosis of low-level mosaic trisomy 17 with maternal uniparental disomy 17 by amniocentesis in a pregnancy with a favorable outcome
by: Chih-Ping Chen, et al.
Published: (2020)

Usefulness of interphase FISH on uncultured amniocytes for rapid confirmation of low-level trisomy 7 mosaicism in a pregnancy with fetal intrauterine growth restriction and microcephaly
by: Chih-Ping Chen, et al.
Published: (2012)

Application of quantitative fluorescent polymerase chain reaction analysis for the rapid confirmation of trisomy 13 of maternal origin in a pregnancy with fetal holoprosencephaly, cyclopia, polydactyly, omphalocele and cell culture failure
by: Chih-Ping Chen, et al.
Published: (2022)

Monozygotic twins discordant for low-level mosaic trisomy 17 at amniocentesis in a pregnancy with a favorable outcome and a literature review of heterokaryotypic monozygotic twins at amniocentesis
by: Chih-Ping Chen, et al.
Published: (2020)

Rapid confirmation of trisomy 13 of maternal origin by QF-PCR following postmortem tissue cell culture failure in a pregnancy with trisomy 13 at amniocentesis and fetal postaxial polydactyly and facial cleft
by: Chih-Ping Chen, et al.
Published: (2022)

Mosaic trisomy 17 at amniocentesis: Prenatal diagnosis, molecular genetic analysis, and literature review
by: Chih-Ping Chen, et al.
Published: (2016)

Rapid diagnosis of trisomy 18 of maternal origin by quantitative fluorescent polymerase chain reaction analysis following tissue culture failure for conventional cytogenetic analysis in a fetus with holoprosencephaly, ventricular septal defect, arthrogryposis of bilateral wrists and aplasia of the thumbs
by: Chih-Ping Chen, et al.
Published: (2021)

Mosaic trisomy 18 at amniocentesis associated with a favorable fetal outcome in a pregnancy
by: Chih-Ping Chen, et al.
Published: (2022)

Tetrasomy of 11q13.4-q14.3 due to an intrachromosomal triplication associated with paternal uniparental isodisomy for 11q14.3-qter, intrauterine growth restriction, developmental delay, corpus callosum dysgenesis, microcephaly, congenital heart defects and facial dysmorphism
by: Chih-Ping Chen, et al.
Published: (2021)

Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetus
by: Chih-Ping Chen, et al.
Published: (2021)

Prenatal diagnosis of mosaic trisomy 18 and maternal uniparental disomy 18 by amniocentesis in a pregnancy associated with cytogenetic discrepancy in various tissues and a favorable fetal outcome
by: Chih-Ping Chen, et al.
Published: (2023)

Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result
by: Chih-Ping Chen, et al.
Published: (2021)

Prenatal diagnosis of low-level mosaicism for trisomy 18 associated with a favorable fetal outcome
by: Chih-Ping Chen, et al.
Published: (2016)

Rapid diagnosis of trisomy 13 of maternal origin by quantitative fluorescent polymerase chain reaction analysis in a pregnancy with fetal holoprosencephaly, premaxillary agenesis, postaxial polydactyly of left hand and overriding aorta
by: Chih-Ping Chen, et al.
Published: (2021)

Prenatal diagnosis of mosaic tetrasomy 18p
by: Chih-Ping Chen, et al.
Published: (2012)

Limb-Body Wall Complex in One Fetus of a Dizygotic Twin Pregnancy Conceived by Egg Donation, In Vitro Fertilization and Embryo Transfer: Prenatal Diagnosis and Literature Review
by: Chih-Ping Chen, et al.
Published: (2009)

Molecular cytogenetic characterization of a de novo chromosome 1q41-q42.11 microdeletion of paternal origin in a 15-year-old boy with mental retardation, developmental delay, autism and congenital heart defects
by: Chih-Ping Chen, et al.
Published: (2021)

Prenatal diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency, mosaicism for de novo multiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader-Willi syndrome
by: Chih-Ping Chen, et al.
Published: (2021)

Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly
by: Chih-Ping Chen, et al.
Published: (2011)

Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 18 at amniocentesis in a pregnancy with a favorable fetal outcome and maternal uniparental disomy 18
by: Chih-Ping Chen, et al.
Published: (2022)

Low-level mosaic trisomy 13 at amniocentesis associated with a favorable outcome in a pregnancy
by: Chih-Ping Chen, et al.
Published: (2020)

Prenatal diagnosis of mosaicism for double aneuploidy of 47,XXY and trisomy 7 (48,XXY,+7) at amniocentesis in a pregnancy with a favorable outcome
by: Chih-Ping Chen, et al.
Published: (2021)

Mosaic trisomy 21 at amniocentesis associated with a favorable fetal outcome and perinatal progressive decrease of the trisomy 21 cell line
by: Chih-Ping Chen, et al.
Published: (2023)

Partial Trisomy 16p (16p12.2→pter) and Partial Monosomy 22q (22q13.31 →qter) Presenting With Fetal Ascites and Ventriculomegaly: Prenatal Diagnosis and Array Comparative Genomic Hybridization Characterization
by: Chih-Ping Chen, et al.
Published: (2010)

Trisomy 13 Mosaicism Associated With Cyclopia and Cystic Hygroma
by: Chih-Ping Chen, et al.
Published: (2009)