Cover Image

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

Objective: To present prenatal diagnosis and molecular cytogenetic characterization of trisomy 18 in a monozygotic twin pregnancy, with one structurally abnormal living fetus and one intrauterine fetal demise. Case Report: A 38-year-old woman was referred for amniocentesis at 16 weeks of gestation b...

Full description

Saved in:

Bibliographic Details
Main Authors:	Chih-Ping Chen (Author), Schu-Rern Chern (Author), Yi-Yung Chen (Author), Pei-Chen Wu (Author), Dai-Dyi Town (Author), Wen-Lin Chen (Author), Wayseen Wang (Author)
Format:	Book
Published:	Elsevier, 2012-09-01T00:00:00Z.
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 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)

Detection of paternal origin of fetal trisomy 18 in a pregnancy conceived by assisted reproductive technology and in vitro fertilization
by: Chih-Ping Chen, et al.
Published: (2020)

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)

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)

Prognosis of remaining fetus in twin pregnancy after demise of one fetus according to its location
by: Young Mi Jung, et al.
Published: (2024)

Prenatal diagnosis of mosaic trisomy 2: Discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction
by: Chih-Ping Chen, et al.
Published: (2011)

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)

Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic double trisomy involving trisomy 7 and trisomy 20 (48,XY,+7,+20) at amniocentesis
by: Chih-Ping Chen, et al.
Published: (2020)

Prenatal diagnosis of mosaic trisomy 8 by amniocentesis in a fetus with ventriculomegaly and dysgenesis of the corpus callosum
by: Chih-Ping Chen, et al.
Published: (2020)

Prenatal diagnosis and management of monozygotic twins discordant for severe fetal abnormalities
by: Chih-Ping Chen, et al.
Published: (2020)

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)

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)

Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis
by: Chih-Ping Chen, et al.
Published: (2020)

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

Prenatal Visualization of Cebocephaly with a Prominent Nose in a Second-trimester Fetus with Alobar Holoprosencephaly and Trisomy 13
by: Chih-Ping Chen, et al.
Published: (2008)

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

Low-level mosaic trisomy 17 at amniocentesis in a pregnancy associated with a favorable fetal outcome and cytogenetic discrepancy between cultured and uncultured amniocytes
by: Chih-Ping Chen, et al.
Published: (2023)

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)

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)

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)

Cytomegalovirus infection and fetal death in one monozygotic twin
by: Hsin-Yi Wu, et al.
Published: (2011)

Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome
by: Chih-Ping Chen, et al.
Published: (2017)

Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion
by: Chih-Ping Chen, et al.
Published: (2016)

Low-level mosaic trisomy 2 at amniocentesis in a pregnancy associated with positive NIPT and CVS results for trisomy 2, maternal uniparental disomy 2, perinatal progressive decrease of the aneuploid cell line, cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, intrauterine growth restriction and a favorable fetal outcome
by: Chih-Ping Chen, et al.
Published: (2023)

Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes
by: Chih-Ping Chen, et al.
Published: (2016)

Discordant anencephaly and Cantrell syndrome in monozygotic twins conceived by ICSI and IVF-ET
by: Chih-Ping Chen, et al.
Published: (2013)

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 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)

Low-level mosaic trisomy 13 at amniocentesis in a pregnancy associated with a positive NIPT result suspicious of trisomy 13, a CVS result of mosaic trisomy 13, cytogenetic discrepancy in various tissues and a favorable fetal outcome
by: Chih-Ping Chen, et al.
Published: (2023)

Mosaic trisomy 16 at amniocentesis in a pregnancy associated with positive non-invasive prenatal testing for trisomy 16, placental trisomy 16, intrauterine growth restriction, intrauterine fetal death, cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, and prenatal progressive decrease of the aneuploid cell line
by: Chih-Ping Chen, et al.
Published: (2023)

Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis in a pregnancy with a favorable outcome
by: Chih-Ping Chen, et al.
Published: (2022)

Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic trisomy 20 at amniocentesis in a pregnancy with a favorable outcome
by: Chih-Ping Chen, et al.
Published: (2022)

Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome
by: Chih-Ping Chen, et al.
Published: (2017)

Low-level mosaic trisomy 9 at amniocentesis in a pregnancy associated with a favorable fetal outcome, intrauterine growth restriction, cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes and perinatal progressive decrease of the aneuploid cell line
by: Chih-Ping Chen, et al.
Published: (2023)

Prenatal Diagnosis and Molecular Analysis of Triploidy in a Fetus With Intrauterine Growth Restriction, Relative Macrocephaly and Holoprosencephaly
by: Chih-Ping Chen, et al.
Published: (2009)

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)

Double aneuploidy with Edwards-Klinefelter syndromes (48,XXY,+18) of maternal origin: Prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis of the left wrist and aplasia of the left thumb
by: Chih-Ping Chen, et al.
Published: (2011)

Low-level mosaic trisomy 13 at amniocentesis in a pregnancy associated with a favorable fetal outcome and cytogenetic discrepancy in various tissues
by: Chih-Ping Chen, et al.
Published: (2023)

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)

Magnetic resonance imaging demonstration of sirenomelia in one fetus of a dizygotic twin pregnancy conceived by intracytoplasmic sperm injection, in vitro fertilization and embryo transfer
by: Chih-Ping Chen, et al.
Published: (2011)