Anophthalmia in a retarded girl with partial trisomy 4p and 22 following a maternal translocation, rcp(4;22)(p15.2;q11.2)

Ophthalmic Paediatr Genet. 1990 Jun;11(2):139-42. doi: 10.3109/13816819009012960.

Abstract

An 18-year-old girl displayed left anophthalmia and right severe microphthalmia, mild dysmorphic features of facies and distal limbs, a right preauricular pit, and moderate mental retardation. She was trisomic for the distal part of the short arm of chromosome 4 and the proximal segment of chromosome 22, due to unbalanced 3:1 segregation of a maternal 4;22-translocation. Anophthalmia is a rare finding in chromosome aberrations in general, and particularly in patients not featuring other severe malformations and severe to profound mental retardation.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Anophthalmos / complications
  • Anophthalmos / genetics*
  • Child
  • Chromosomes, Human, Pair 22*
  • Chromosomes, Human, Pair 4*
  • Female
  • Humans
  • Intellectual Disability / complications*
  • Intellectual Disability / genetics
  • Karyotyping
  • Male
  • Microphthalmos / complications
  • Microphthalmos / genetics
  • Translocation, Genetic*
  • Trisomy*