Ocular coloboma

Surv Ophthalmol. Jan-Feb 1981;25(4):223-36. doi: 10.1016/0039-6257(81)90092-8.

Abstract

Ocular coloboma is common malformation which includes a spectrum of anomalies that ranges from iris coloboma to clinical anophthalmos. Coloboma is etiologically heterogeneous. As an isolated defect, it is usually inherited as an autosomal dominant disorder, although autosomal recessive inheritance also occurs. Patients with multiple malformations and coloboma may have a recognized malformation syndrome of unknown etiology, a single gene disorder, or chromosomal abnormality. Prognosis and recurrence risk can be determined only after complete evaluation of the patient and other family members.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Child
  • Choroid / abnormalities
  • Coloboma / genetics*
  • Eye / embryology
  • Eye Abnormalities*
  • Female
  • Genes, Dominant
  • Genes, Recessive
  • Humans
  • Infant
  • Iris / abnormalities*
  • Male
  • Retina / abnormalities