Karyotyping for isolated neural tube defects

A report of two cases

Geralyn O'Reilly, L. E. Shields

Research output: Contribution to journalArticle

Abstract

BACKGROUND: Neural tube defects occur in approximately 1 in every 1,000 live births. In the United States, chromosomal abnormalities have been noted in 2-10% of fetuses with neural tube defects; however, there is no consensus on whether to offer karyotype analysis to patients with isolated neural tube defects found on ultrasound. CASE: We reviewed the prenatal diagnosis database for the University of Washington between 1985 and 1997. We report on two fetuses who, on ultrasound, were found to have 'isolated' neural tube defects. Karyotype analysis revealed trisomy 18 in both fetuses. The pregnancies were subsequently terminated, and autopsy revealed subtle syndromic findings that were not identified on ultrasound. CONCLUSION: Fetuses with isolated neural tube defects also appear to have a high risk of chromosomal abnormalities, so patients should be offered fetal karyotyping to define recurrence risks for future pregnancies.

Original languageEnglish (US)
Pages (from-to)950-952
Number of pages3
JournalJournal of Reproductive Medicine for the Obstetrician and Gynecologist
Volume45
Issue number11
StatePublished - Dec 12 2000
Externally publishedYes

Fingerprint

Karyotyping
Neural Tube Defects
Fetus
Karyotype
Chromosome Aberrations
Pregnancy
Live Birth
Prenatal Diagnosis
Autopsy
Databases
Recurrence

Keywords

  • Karyotyping
  • Neural tube defects
  • Pregnancy complications

ASJC Scopus subject areas

  • Obstetrics and Gynecology
  • Reproductive Medicine

Cite this

Karyotyping for isolated neural tube defects : A report of two cases. / O'Reilly, Geralyn; Shields, L. E.

In: Journal of Reproductive Medicine for the Obstetrician and Gynecologist, Vol. 45, No. 11, 12.12.2000, p. 950-952.

Research output: Contribution to journalArticle

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