Literature DB >> 3355418

Variable expressivity of autosomal dominant microcornea with cataract.

J F Salmon1, C E Wallis, A D Murray.   

Abstract

Autosomal dominant microcornea with a cataract, previously described in four families, was documented in a seven-generation family. Eighteen family members had microcornea and a cataract, and an additional six had sclerocornea or Peters' anomaly. Most individuals with microcornea had a corneal diameter of less than 11 mm in both meridians, with moderately steep corneal curvatures. The inherited cataract progressed to form a total cataract after visual maturity had been achieved. In the four affected children who had not undergone cataract extraction, the common abnormality was a posterior polar lens opacity. The variability of expressivity of the dominant gene would suggest that the embryological origins of microcornea and sclerocornea are similar.

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Year:  1988        PMID: 3355418     DOI: 10.1001/archopht.1988.01060130551034

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN: 0003-9950


  9 in total

Review 1.  Genetics of aniridia and anterior segment dysgenesis.

Authors:  A Churchill; A Booth
Journal:  Br J Ophthalmol       Date:  1996-07       Impact factor: 4.638

2.  Bilateral congenital dentiform cataract and extreme microcornea in eyes with uveal colobomas and persistent hyperplastic primary vitreous.

Authors:  B Seitz; G O Naumann
Journal:  Br J Ophthalmol       Date:  1996-04       Impact factor: 4.638

3.  Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.

Authors:  R A Lewis
Journal:  Trans Am Ophthalmol Soc       Date:  1989

Review 4.  Genetic modifiers as relevant biological variables of eye disorders.

Authors:  Kacie J Meyer; Michael G Anderson
Journal:  Hum Mol Genet       Date:  2017-08-01       Impact factor: 6.150

5.  An unusual pedigree with microcornea-cataract syndrome.

Authors:  E Stefaniak; J Zaremba; I Cieślińska; E Kropińska
Journal:  J Med Genet       Date:  1995-10       Impact factor: 6.318

6.  Pulverulent cataract with variably associated microcornea and iris coloboma in a MAF mutation family.

Authors:  R V Jamieson; F Munier; A Balmer; N Farrar; R Perveen; G C M Black
Journal:  Br J Ophthalmol       Date:  2003-04       Impact factor: 4.638

7.  Heterogeneity in dominant anterior segment malformations.

Authors:  G E Holmström; W P Reardon; M Baraitser; J S Elston; D S Taylor
Journal:  Br J Ophthalmol       Date:  1991-10       Impact factor: 4.638

8.  Novel human CRYGD rare variant in a Brazilian family with congenital cataract.

Authors:  Eugênio Santana de Figueirêdo; Gabriel Gorgone Giordano; Anderson Tavares; Márcio José da Silva; José Paulo Cabral de Vasconcellos; Carlos Eduardo Leite Arieta; Mônica Barbosa de Melo
Journal:  Mol Vis       Date:  2011-08-16       Impact factor: 2.367

9.  Cataract surgery for tilted lens in peters' anomaly type 2.

Authors:  Tadayuki Nishide; Misako Nakanishi; Natsuki Hayakawa; Ikuko Kimura; Nobuhisa Mizuki
Journal:  Case Rep Ophthalmol       Date:  2013-09-26
  9 in total

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