Sacral dysgenesis associated with terminal deletion of chromosome 7 (q36-qter)

Pediatr Neonatol. 2008 Oct;49(5):189-92. doi: 10.1016/S1875-9572(09)60007-3.

Abstract

We report on the clinical, cytogenetic, and imaging findings in a patient with a 7q terminal deletion. The 11-year-old girl had mental retardation, microcephaly, a distinctive face, relatively small hands and feet, and sacral dysgenesis. High resolution GTG banding (550-850 bands) showed a 7q terminal deletion. A detailed evaluation of associated malformations and the overall clinical picture should be taken into account when identifying the underlying diagnosis in cases of sacral dysgenesis with mental retardation.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple
  • Child
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 7*
  • Female
  • Humans
  • Sacrum / abnormalities*