Unilateral Peters' anomaly in an infant with 22q11.2 deletion syndrome

Clin Dysmorphol. 2008 Oct;17(4):289-90. doi: 10.1097/MCD.0b013e3283079e7c.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics
  • Abnormalities, Multiple / pathology*
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22*
  • Eye Abnormalities / genetics
  • Eye Abnormalities / pathology*
  • Genetic Diseases, Inborn / genetics
  • Genetic Diseases, Inborn / pathology*
  • Humans
  • Infant
  • Male
  • Syndrome