Congenital glaucoma associated with 22p+ variant in a dysmorphic child

Indian J Ophthalmol. 2003 Dec;51(4):355-7.

Abstract

A case of congenital glaucoma with developmental delay and several dysmorphic features showing 22p+ chromosomal variant is reported.

Publication types

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

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosome Aberrations*
  • Chromosomes, Human, Pair 22 / genetics*
  • Craniofacial Abnormalities / genetics*
  • Glaucoma / congenital*
  • Humans
  • Infant
  • Intraocular Pressure
  • Karyotyping
  • Male
  • Nucleolus Organizer Region / pathology