Second-trimester diagnosis of complete trisomy 9 associated with abnormal maternal serum screen results, open sacral spina bifida and congenital diaphragmatic hernia, and review of the literature

Chih Ping Chen, Schu Rern Chern, Sho Jen Cheng, Tung Yao Chang, Li Fan Yeh, Chen Chi Lee, Chen Wen Pan, Wayseen Wang, Chin Yuan Tzen

Research output: Contribution to journalReview article

29 Citations (Scopus)

Abstract

Objectives: To present the prenatal diagnosis of complete trisomy 9 and to review the literature. Case: A 25-year-old primigravida woman was referred for amniocentesis at 19 weeks' gestation because of abnormal maternal screen results showing an elevated maternal serum alpha-fetoprotein (MSAFP) level and a low maternal serum free β-human chorionic gonadotrophin (MSfreeβ-hCG) level. Results: Genetic amniocentesis revealed a karyotype of 47,XX,+9 in the amniocytes and an elevated amniotic fluid AFP level. Ultrasonography demonstrated intrauterine growth restriction, left congenital diaphragmatic hernia, fetal ascites, a sacral spina bifida, a horseshoe kidney, and absence of amniotic fluid. Ultrafast magnetic resonance imaging scans further depicted detailed anatomical configurations of the major congenital malformations. The pregnancy was terminated subsequently. The proband postnatally manifested characteristic facial dysmorphism, limb deformities, and an open sacral spina bifida with myelomeningocele. Cytogenetic analysis of the skin fibroblasts revealed a karyotype of 47,XX,+9. Molecular studies of various uncultured fetal tissues using microsatellite markers confirmed a diagnosis of complete trisomy 9 resulting from a meiotic I nondisjunction error of maternal origin. Conclusion: Complete trisomy 9 can be identified prenatally with advanced maternal age, sonographically detected fetal structural abnormalities, and abnormal maternal serum screen results. Fetuses with complete trisomy 9 may be associated with congenital diaphragmatic hernia, an open sacral spina bifida, elevated MSAFP, and low MSfreeβ-hCG. We suggest detailed prenatal imaging investigations and genetic analyses of multiple fetal tissues when a prenatal diagnosis of trisomy 9 is made.

Original languageEnglish
Pages (from-to)455-462
Number of pages8
JournalPrenatal Diagnosis
Volume24
Issue number6
DOIs
Publication statusPublished - Jun 1 2004
Externally publishedYes

Fingerprint

Spina Bifida Cystica
Second Pregnancy Trimester
Mothers
Serum
Fetus
Amniocentesis
alpha-Fetoproteins
Chorionic Gonadotropin
Amniotic Fluid
Prenatal Diagnosis
Karyotype
Meningomyelocele
Pregnancy
Spinal Dysraphism
Cytogenetic Analysis
Maternal Age
Congenital Diaphragmatic Hernias
Trisomy Chromosome 9
Ascites
Microsatellite Repeats

Keywords

  • Complete trisomy 9
  • Congenital diaphragmatic hernia
  • Maternal serum screen
  • Neural tube defects
  • Prenatal diagnosis

ASJC Scopus subject areas

  • Obstetrics and Gynaecology
  • Genetics(clinical)

Cite this

Second-trimester diagnosis of complete trisomy 9 associated with abnormal maternal serum screen results, open sacral spina bifida and congenital diaphragmatic hernia, and review of the literature. / Chen, Chih Ping; Chern, Schu Rern; Cheng, Sho Jen; Chang, Tung Yao; Yeh, Li Fan; Lee, Chen Chi; Pan, Chen Wen; Wang, Wayseen; Tzen, Chin Yuan.

In: Prenatal Diagnosis, Vol. 24, No. 6, 01.06.2004, p. 455-462.

Research output: Contribution to journalReview article

Chen, Chih Ping ; Chern, Schu Rern ; Cheng, Sho Jen ; Chang, Tung Yao ; Yeh, Li Fan ; Lee, Chen Chi ; Pan, Chen Wen ; Wang, Wayseen ; Tzen, Chin Yuan. / Second-trimester diagnosis of complete trisomy 9 associated with abnormal maternal serum screen results, open sacral spina bifida and congenital diaphragmatic hernia, and review of the literature. In: Prenatal Diagnosis. 2004 ; Vol. 24, No. 6. pp. 455-462.
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abstract = "Objectives: To present the prenatal diagnosis of complete trisomy 9 and to review the literature. Case: A 25-year-old primigravida woman was referred for amniocentesis at 19 weeks' gestation because of abnormal maternal screen results showing an elevated maternal serum alpha-fetoprotein (MSAFP) level and a low maternal serum free β-human chorionic gonadotrophin (MSfreeβ-hCG) level. Results: Genetic amniocentesis revealed a karyotype of 47,XX,+9 in the amniocytes and an elevated amniotic fluid AFP level. Ultrasonography demonstrated intrauterine growth restriction, left congenital diaphragmatic hernia, fetal ascites, a sacral spina bifida, a horseshoe kidney, and absence of amniotic fluid. Ultrafast magnetic resonance imaging scans further depicted detailed anatomical configurations of the major congenital malformations. The pregnancy was terminated subsequently. The proband postnatally manifested characteristic facial dysmorphism, limb deformities, and an open sacral spina bifida with myelomeningocele. Cytogenetic analysis of the skin fibroblasts revealed a karyotype of 47,XX,+9. Molecular studies of various uncultured fetal tissues using microsatellite markers confirmed a diagnosis of complete trisomy 9 resulting from a meiotic I nondisjunction error of maternal origin. Conclusion: Complete trisomy 9 can be identified prenatally with advanced maternal age, sonographically detected fetal structural abnormalities, and abnormal maternal serum screen results. Fetuses with complete trisomy 9 may be associated with congenital diaphragmatic hernia, an open sacral spina bifida, elevated MSAFP, and low MSfreeβ-hCG. We suggest detailed prenatal imaging investigations and genetic analyses of multiple fetal tissues when a prenatal diagnosis of trisomy 9 is made.",
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AU - Chen, Chih Ping

AU - Chern, Schu Rern

AU - Cheng, Sho Jen

AU - Chang, Tung Yao

AU - Yeh, Li Fan

AU - Lee, Chen Chi

AU - Pan, Chen Wen

AU - Wang, Wayseen

AU - Tzen, Chin Yuan

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N2 - Objectives: To present the prenatal diagnosis of complete trisomy 9 and to review the literature. Case: A 25-year-old primigravida woman was referred for amniocentesis at 19 weeks' gestation because of abnormal maternal screen results showing an elevated maternal serum alpha-fetoprotein (MSAFP) level and a low maternal serum free β-human chorionic gonadotrophin (MSfreeβ-hCG) level. Results: Genetic amniocentesis revealed a karyotype of 47,XX,+9 in the amniocytes and an elevated amniotic fluid AFP level. Ultrasonography demonstrated intrauterine growth restriction, left congenital diaphragmatic hernia, fetal ascites, a sacral spina bifida, a horseshoe kidney, and absence of amniotic fluid. Ultrafast magnetic resonance imaging scans further depicted detailed anatomical configurations of the major congenital malformations. The pregnancy was terminated subsequently. The proband postnatally manifested characteristic facial dysmorphism, limb deformities, and an open sacral spina bifida with myelomeningocele. Cytogenetic analysis of the skin fibroblasts revealed a karyotype of 47,XX,+9. Molecular studies of various uncultured fetal tissues using microsatellite markers confirmed a diagnosis of complete trisomy 9 resulting from a meiotic I nondisjunction error of maternal origin. Conclusion: Complete trisomy 9 can be identified prenatally with advanced maternal age, sonographically detected fetal structural abnormalities, and abnormal maternal serum screen results. Fetuses with complete trisomy 9 may be associated with congenital diaphragmatic hernia, an open sacral spina bifida, elevated MSAFP, and low MSfreeβ-hCG. We suggest detailed prenatal imaging investigations and genetic analyses of multiple fetal tissues when a prenatal diagnosis of trisomy 9 is made.

AB - Objectives: To present the prenatal diagnosis of complete trisomy 9 and to review the literature. Case: A 25-year-old primigravida woman was referred for amniocentesis at 19 weeks' gestation because of abnormal maternal screen results showing an elevated maternal serum alpha-fetoprotein (MSAFP) level and a low maternal serum free β-human chorionic gonadotrophin (MSfreeβ-hCG) level. Results: Genetic amniocentesis revealed a karyotype of 47,XX,+9 in the amniocytes and an elevated amniotic fluid AFP level. Ultrasonography demonstrated intrauterine growth restriction, left congenital diaphragmatic hernia, fetal ascites, a sacral spina bifida, a horseshoe kidney, and absence of amniotic fluid. Ultrafast magnetic resonance imaging scans further depicted detailed anatomical configurations of the major congenital malformations. The pregnancy was terminated subsequently. The proband postnatally manifested characteristic facial dysmorphism, limb deformities, and an open sacral spina bifida with myelomeningocele. Cytogenetic analysis of the skin fibroblasts revealed a karyotype of 47,XX,+9. Molecular studies of various uncultured fetal tissues using microsatellite markers confirmed a diagnosis of complete trisomy 9 resulting from a meiotic I nondisjunction error of maternal origin. Conclusion: Complete trisomy 9 can be identified prenatally with advanced maternal age, sonographically detected fetal structural abnormalities, and abnormal maternal serum screen results. Fetuses with complete trisomy 9 may be associated with congenital diaphragmatic hernia, an open sacral spina bifida, elevated MSAFP, and low MSfreeβ-hCG. We suggest detailed prenatal imaging investigations and genetic analyses of multiple fetal tissues when a prenatal diagnosis of trisomy 9 is made.

KW - Complete trisomy 9

KW - Congenital diaphragmatic hernia

KW - Maternal serum screen

KW - Neural tube defects

KW - Prenatal diagnosis

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