Literature DB >> 677223

Persistent pupillary membrane associated with aniridia.

N Hamming, J Wilensky.   

Abstract

Familial aniridia is an autosomal dominant condition in which only a small iris remnant is present. A controversy exists as to whether the pathogenetic, embryologic origin of this condition is neuroectodermal or mesodermal. We examined a male infant with bilateral congenital aniridia associated with persistent pupillary membranes. This child had a prominent arcade of vessels extending onto the anterior lens surface for 360 degrees from small iris remnants in both eyes. The presence of a mesodermal pupillary membrane despite absence of the iris suggested a primary neuroectodermal defect as the pathogenetic factor in this case of aniridia.

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Mesh:

Year:  1978        PMID: 677223     DOI: 10.1016/0002-9394(78)90027-2

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  4 in total

1.  Conservative management of bilateral persistent pupillary membranes with 18 years of follow-up.

Authors:  Birthe Meyer-Rüsenberg; Michelle Thill; Snjezana Vujancevic; Hans-Werner Meyer-Rüsenberg
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2010-02-25       Impact factor: 3.117

2.  Remnants of the anterior tunica vasculosa lentis and long anterior lens zonules.

Authors:  Daniel K Roberts; Tricia L Newman; Mary F Roberts; Jacob T Wilensky
Journal:  J Glaucoma       Date:  2014-09       Impact factor: 2.503

3.  Persistent anterior tunica vasculosa lentis in multisystemic smooth muscle dysfunction syndrome: A case report.

Authors:  Kaiqin She; Licong Liang; Fang Lu
Journal:  Medicine (Baltimore)       Date:  2021-06-04       Impact factor: 1.817

4.  [Infant with bilateral corneal opacity and aniridia].

Authors:  Helena Wagner; Uta Matysiak; Wolf A Lagrèze
Journal:  Ophthalmologe       Date:  2020-11       Impact factor: 1.059

  4 in total

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