Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

Congenital ectopic pupil

Known as: Ectopic pupil, Ectopia pupillae, Corectopia 
A malposition of the pupil owing to a developmental defect of the iris. [DDD:gblack, HPO:probinson]
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Anterior segment dysgeneses (ASDs) comprise a spectrum of developmental disorders affecting the anterior segment of the eye. Here… Expand
  • figure 1
  • table 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
2013
2013
PURPOSE To investigate the diverse ocular manifestations and identify the causative mutation in a large family with autosomal… Expand
Is this relevant?
Highly Cited
2011
Highly Cited
2011
OBJECTIVES To identify CRB1 mutations in a large cohort of patients with recessive retinal dystrophies and to document the… Expand
  • table 1
  • table 2
  • table 3
  • figure 1
  • figure 2
Is this relevant?
2011
2011
PurposeTo evaluate the surgical outcome of combined trabeculotomy–trabeculectomy in Ghanaian children with primary congenital… Expand
  • figure 1
  • figure 2
  • figure 3
  • table 1
Is this relevant?
2009
2009
INTRODUCTION Buccally displaced canines (BDC) are usually found in crowded dentitions. Nevertheless, a small but significant… Expand
  • figure 1
  • figure 2
  • table I
  • table II
  • table III
Is this relevant?
2007
2007
PAX6 is a key regulator of eye development and there are many well recognized ophthalmic sequelae of mutations at this locus. The… Expand
Is this relevant?
2006
2006
In eye aberrometry it is often necessary to transform the aberration coefficients in order to express them in a scaled, rotated… Expand
Is this relevant?
2002
2002
Axenfeld-Rieger anomaly (ARA) is an autosomal dominant disorder of the anterior chamber of the eye that includes a prominent and… Expand
Is this relevant?
2001
2001
PURPOSE Rieger syndrome is an autosomal dominant condition defined by anterior segment dysgenesis in combination with facial… Expand
Is this relevant?
Highly Cited
1999
Highly Cited
1999
Mutations of the human PAX6 gene underlie aniridia (congenital absence of the iris), a rare dominant malformation of the eye. The… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?