Ring chromosome 15 in a patient with features of Fryns' syndrome

J Med Genet. 1989 Jul;26(7):469-70. doi: 10.1136/jmg.26.7.469.

Abstract

A stillborn male infant with a ring chromosome 15 and some features compatible with Fryns' syndrome is presented. Neither diagnosis is common and the overlap may be of significance.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosome Aberrations*
  • Chromosomes, Human, Pair 15* / ultrastructure
  • Female
  • Fetal Death
  • Humans
  • Infant, Newborn
  • Karyotyping
  • Male
  • Pregnancy
  • Ring Chromosomes*
  • Syndrome