Objective: To construct a normal range for the nuchal translucency mea
surement in chromosomally and phenotypically normal fetuses between 9
and 14 weeks' gestation. Methods: The nuchal translucency was measured
prospectively in 771 chromosomally normal fetuses of women attending
our antenatal clinic or prenatal diagnosis center. The nuchal transluc
ency measurement was expressed as the median and fifth, 25th, 75th, an
d 95th percentiles according to completed weeks of gestation based on
ultrasound measurements. Results: The median nuchal translucency measu
rement increased from 0.7 mm at 10 weeks' gestation to 1.5 mm at 13 we
eks. A nuchal translucency measurement greater than 2.5 mm was found i
n 4.6% of the fetuses at 10 weeks' gestation; the incidence increased
to 8.7% at 14 weeks. Conclusion: In normal fetuses, there is a physiol
ogic variation in the nuchal translucency measurement between 9 and 14
weeks' gestation. The calculation of risk for trisomies based on this
measurement should take this variation into account. The adoption of
a gestational age-dependent cutoff point, based on the deviation of a
given measurement from the median, may reduce the number of false-posi
tive test results requiring invasive procedures for karyotyping.