Intrauterine diagnosis and evolution of a cardiomyopathy in a fetus with Noonan's syndrome

Acta Paediatr. 1992 Apr;81(4):368-70. doi: 10.1111/j.1651-2227.1992.tb12247.x.

Abstract

We report on a newborn infant with a typical form of Noonan's syndrome. Because of the presence of a fetal cystic hygroma and normal karyotype the diagnosis was suspected before birth. A progressive hypertrophic cardiomyopathy was also found following fetal echocardiographic scanning. We conclude that in addition to cystic hygroma with normal karyotype, the presence of functional or morphological evidence of myocardial abnormality should be included also as prenatal features of Noonan's syndrome.

Publication types

  • Case Reports

MeSH terms

  • Cardiomyopathy, Hypertrophic / complications
  • Cardiomyopathy, Hypertrophic / congenital
  • Cardiomyopathy, Hypertrophic / diagnostic imaging*
  • Diagnosis, Differential
  • Echocardiography / standards*
  • Female
  • Humans
  • Infant, Newborn
  • Noonan Syndrome / complications
  • Noonan Syndrome / diagnostic imaging*
  • Noonan Syndrome / pathology
  • Pregnancy
  • Ultrasonography, Prenatal / standards*