Prenatal detection of a subtle unbalanced chromosome rearrangement by karyotyping, FISH and array comparative genomic hybridization

Colyn Cargile Cain, Daniel O. Saul, Erin Oehler, Karin Blakemore, Gail Stetten

Research output: Contribution to journalArticle

Abstract

Objectives: To explore the advantages and limitations of comparative genomic hybridization to BAC arrays (array CGH) for prenatal diagnosis of a fetus with anomalies and a chromosome abnormality. Methods: We used karyotype analysis, FISH and array CGH to investigate an unbalanced chromosome rearrangement. Results: We report a case of a fetus with ultrasound anomalies at 11 weeks' gestation and an unbalanced chromosome translocation [46,XX,der(13)t(2;13)(p25.1;q32)pat]. Initially, a chromosome 13 deletion was reported from G-banded chromosome analysis and 13q subtelomere FISH. The involvement of chromosome 2 was determined after a balanced translocation was identified in the father, 46,XY,t(2;13)(p25.1;q32). Array CGH confirmed the fetal abnormality as partial trisomy of the short arm chromosome 2 and partial monosomy of the long arm of chromosome 13. The abnormalities identified by ultrasound studies and autopsy appear to be most consistent with 13q deletion syndrome. Conclusions: Array CGH successfully identified a subtle unbalanced chromosome complement in a fetus with multiple ultrasound anomalies. If array CGH had been performed along with the fetal karyotype, the cryptic partial trisomy 2 could have been identified in a more timely manner to assist in the prenatal counseling of this family.

Original languageEnglish (US)
Pages (from-to)286-290
Number of pages5
JournalFetal Diagnosis and Therapy
Volume24
Issue number3
DOIs
StatePublished - Oct 2008

Fingerprint

Karyotyping
Comparative Genomic Hybridization
Fetus
Chromosomes, Human, Pair 2
Chromosomes
Trisomy
Karyotype
Chromosomes, Human, 21-22 and Y
Chromosomes, Human, Pair 13
Chromosome Deletion
Prenatal Diagnosis
Fathers
Chromosome Aberrations
Counseling
Autopsy
Pregnancy

Keywords

  • 13q deletion syndrome
  • Array comparative genomic hybridization
  • Chromosome translocation
  • FISH

ASJC Scopus subject areas

  • Obstetrics and Gynecology
  • Pediatrics, Perinatology, and Child Health
  • Embryology
  • Radiology Nuclear Medicine and imaging

Cite this

Prenatal detection of a subtle unbalanced chromosome rearrangement by karyotyping, FISH and array comparative genomic hybridization. / Cain, Colyn Cargile; Saul, Daniel O.; Oehler, Erin; Blakemore, Karin; Stetten, Gail.

In: Fetal Diagnosis and Therapy, Vol. 24, No. 3, 10.2008, p. 286-290.

Research output: Contribution to journalArticle

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