9p-Syndrome

J Postgrad Med. 1994 Jan-Mar;40(1):40-1.

Abstract

A 2 1/2 month old male child was admitted with loose motions and mild dehydration. He was full term normal delivery, born of a non-consanguinous marriage. On examination, he had trigonocephaly; anteverted nostrils, long philtrum and hypoplastic supraorbital ridges. X-ray showed sutural separation. Karyotyping confirmed deletion of short arm of chromosome 9 distal to band p22.

Publication types

  • Case Reports

MeSH terms

  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 9*
  • Craniofacial Dysostosis* / etiology
  • Craniofacial Dysostosis* / pathology
  • Humans
  • Male
  • Skull / abnormalities*
  • Syndrome