Literature DB >> 8963810

Videokeratography of keratoconus in monozygotic twins.

J Parker1, W W Ko, G Pavlopoulos, P J Wolfe, Y S Rabinowitz, S T Feldman.   

Abstract

PURPOSE: To determine the corneal topographic appearance in a pair of monozygotic twins and family members of the twins because one of the twins had keratoconus and the other appeared normal by clinical examination.
METHODS: Clinical examination and videokeratography (Topographic Modeling System, Tomey) of the patient, his monozygotic twin brother, an older brother, and his parents were performed. The I-S values (difference in the average dioptric powers of symmetrical points between the inferior and superior cornea) were calculated.
RESULTS: The patient, a 28-year-old man, had clinical keratoconus confirmed with videokeratography. Clinical examination of family members including a twin brother, an older brother and both parents revealed no corneal abnormalities. Videokeratography of the clinically normal twin brother showed inferior steepening with progression over time. The I-S value of the clinically normal brother was 1.36 (right eye) (greater than 2.00 SD of normal controls), which progressed to 1.69 (right eye), 1.32 (left eye) 5 months later and to 1.87 (right eye), 1.43 diopters (D) (left eye) 14 months later. Minimal asymmetric inferior steepening was noted in an older brother who had an I-S value of 0.81 (right eye), 1.27 (left eye). The mother appeared topographically normal.
CONCLUSIONS: This study lends support to the existence of subclinical keratoconus detectable by videokeratography only.

Entities:  

Mesh:

Year:  1996        PMID: 8963810     DOI: 10.3928/1081-597X-19960101-31

Source DB:  PubMed          Journal:  J Refract Surg        ISSN: 1081-597X            Impact factor:   3.573


  14 in total

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2.  Anterior pituitary, sex hormones, and keratoconus: Beyond traditional targets.

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Journal:  Prog Retin Eye Res       Date:  2021-11-02       Impact factor: 19.704

3.  VSX1 gene variants are associated with keratoconus in unrelated Korean patients.

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Journal:  J Hum Genet       Date:  2008-07-15       Impact factor: 3.172

Review 4.  The genetic and environmental factors for keratoconus.

Authors:  Ariela Gordon-Shaag; Michel Millodot; Einat Shneor; Yutao Liu
Journal:  Biomed Res Int       Date:  2015-05-17       Impact factor: 3.411

Review 5.  Gene therapy in keratoconus.

Authors:  Mahgol Farjadnia; Mohammad Naderan; Mehrdad Mohammadpour
Journal:  Oman J Ophthalmol       Date:  2015 Jan-Apr

6.  Pathogenic alleles in microtubule, secretory granule and extracellular matrix-related genes in familial keratoconus.

Authors:  Vishal Shinde; Nara Sobreira; Elizabeth S Wohler; George Maiti; Nan Hu; Giuliana Silvestri; Sonia George; Jonathan Jackson; Aravinda Chakravarti; Colin E Willoughby; Shukti Chakravarti
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7.  Interleukin 1 beta promoter polymorphism is associated with keratoconus in a Japanese population.

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8.  Lack of association between polymorphisms of the DNA base excision repair genes MUTYH and hOGG1 and keratoconus in a Polish subpopulation.

Authors:  Ewelina Synowiec; Katarzyna A Wójcik; Anna Czubatka; Piotr Polakowski; Justyna Izdebska; Jerzy Szaflik; Janusz Błasiak; Jacek P Szaflik
Journal:  Arch Med Sci       Date:  2015-10-12       Impact factor: 3.318

Review 9.  Genetic and genomic perspective to understand the molecular pathogenesis of keratoconus.

Authors:  Nallathambi Jeyabalan; Rohit Shetty; Anuprita Ghosh; Venkata Ramana Anandula; Arka Subhra Ghosh; Govindasamy Kumaramanickavel
Journal:  Indian J Ophthalmol       Date:  2013-08       Impact factor: 1.848

10.  Polymorphisms of the homologous recombination gene RAD51 in keratoconus and Fuchs endothelial corneal dystrophy.

Authors:  Ewelina Synowiec; Katarzyna A Wojcik; Justyna Izdebska; Ewelina Binczyk; Janusz Blasiak; Jerzy Szaflik; Jacek P Szaflik
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