Ring chromosome 7 and sacral agenesis

Am J Med Genet. 2000 Sep 4;94(1):52-8. doi: 10.1002/1096-8628(20000904)94:1<52::aid-ajmg11>3.0.co;2-q.

Abstract

A ring chromosome 7 was found in a 19-month-old girl with microcephaly, growth and developmental delay, multiple angiomas, and partial sacral agenesis. Absent sacrum is a frequent finding in patients with 7q terminal deletions; in fact, genes involved in the sacral agenesis are localized in 7q36. However, this anomaly was not described previously in patients with a ring chromosome 7. High resolution G-banding chromosome and fluorescence in situ hybridization (FISH) demonstrated that our patient lost this region during ring formation.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosome Aberrations*
  • Chromosome Disorders*
  • Chromosomes, Human, Pair 7*
  • Female
  • Hemangioma / genetics
  • Humans
  • Infant
  • Karyotyping
  • Microcephaly / genetics
  • Mosaicism / genetics
  • Ring Chromosomes*
  • Sacrococcygeal Region / abnormalities*