IUGR IN TRISOMY 18  

The prevalence of IUGR in fetuses with trisomy 18 increases with gestational age.

The cycle time for cell growth and division is longer for trisomic cells than for cells with a normal karyotype. The slower rate of cell growth explains the growth restriction detected on antenatal sonography (3).

The survival rate for trisomy 18 fetuses that have a normal diploid cell line in their placenta is better than those fetuses that have a mosaic trisomy 18 placenta.

Trisomy 18 fetuses with a nonmosaic trisomy 18 placenta always result in an embryonic or fetal demise (4).

 

ULTRASOUND


 

Link to Ultrasound in the Diagnosis of IUGR

 

 

 

REFERENCES

  1. Nyberg DA, Kramer D, Resta RG et.al. Prenatal sonographic findings of trisomy 18: review of 47 cases. J Ultrasound Med 1993;2:103-113.
  2. Kuhn P, de Lourdes Brizot M, Pandya PP et.al. Crown-rump length in chromosomally abnormal fetuses at 10-13 weeks gestation Am J Obstet Gynecol 1995;172:32-35.
  3. Paton GR, Silveo MF, Allison AC. Comparison of cell cycle time in normal and trisomic fetuses. Humangenetik 1974;23:173-182.
  4. Kalousek DK, Barrett IJ, McGillvray BC. Placental mosaicism and intrauterine survival of trisomies 13 and 18. Am J Hun Genet 1989;44:338-343.