Literature DB >> 9924333

Severe form of juvenile corneal stromal dystrophy with homozygous R124H mutation in the keratoepithelin gene in five Japanese patients.

Y Mashima1, M Konishi, Y Nakamura, Y Imamura, M Yamada, T Ogata, J Kudoh, N Shimizu.   

Abstract

AIM: To confirm the mutation of the keratoepithelin gene in patients with a severe form of superficial juvenile granular corneal dystrophy (GCD).
METHODS: Five Japanese probands in whom GCD was diagnosed after histopathological examination and who developed severe manifestations of GCD in their first decade of life were investigated. Other affected family members of two probands were also examined. All probands were the offspring of consanguineous parents. DNA was extracted from their peripheral blood leucocytes and mutational analysis of the gene was performed by the polymerase chain reaction and direct sequencing.
RESULTS: Four of the five probands underwent their first keratectomy or keratoplasty in their teens and subsequently underwent a second or third keratoplasty. Each proband had a homozygous G-->A transition at codon 124, replacing Arg-->His, of the keratoepithelin gene. Their moderately affected family members were heterozygous for the mutation.
CONCLUSIONS: This finding suggests that the severity of the corneal phenotype depends on the dose effect of the mutant gene.

Entities:  

Mesh:

Year:  1998        PMID: 9924333      PMCID: PMC1722402          DOI: 10.1136/bjo.82.11.1280

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


  18 in total

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Journal:  Nippon Ganka Gakkai Zasshi       Date:  1977-01-10

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Authors:  H U Møller; A E Ridgway
Journal:  Acta Ophthalmol (Copenh)       Date:  1990-02

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Authors:  A Garner
Journal:  Br J Ophthalmol       Date:  1969-12       Impact factor: 4.638

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Journal:  Arch Ophthalmol       Date:  1970-08

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Authors:  R Haddad; R L Font; B S Fine
Journal:  Am J Ophthalmol       Date:  1977-02       Impact factor: 5.258

8.  Clinically atypical granular corneal dystrophy with pathologic features of lattice-like amyloid deposits. A study of these families.

Authors:  R Folberg; E Alfonso; J O Croxatto; N G Driezen; N Panjwani; P R Laibson; S A Boruchoff; J Baum; E S Malbran; R Fernandez-Meijide
Journal:  Ophthalmology       Date:  1988-01       Impact factor: 12.079

9.  Avellino corneal dystrophy. Clinical manifestations and natural history.

Authors:  E J Holland; S M Daya; E M Stone; R Folberg; A A Dobler; J D Cameron; D J Doughman
Journal:  Ophthalmology       Date:  1992-10       Impact factor: 12.079

10.  Superficial juvenile granular dystrophy.

Authors:  S H Sajjadi; M A Javadi
Journal:  Ophthalmology       Date:  1992-01       Impact factor: 12.079

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  12 in total

1.  Homozygous mutation (L527R) of TGFBI in an individual with lattice corneal dystrophy.

Authors:  N Yamada; T-I Chikama; N Morishige; R Yanai; T Nishida; M Inui; K Seki
Journal:  Br J Ophthalmol       Date:  2005-06       Impact factor: 4.638

2.  Corneal electrolysis for recurrence of corneal stromal dystrophy after keratoplasty.

Authors:  Y Mashima; M Kawai; M Yamada
Journal:  Br J Ophthalmol       Date:  2002-03       Impact factor: 4.638

3.  Genotype-phenotype correlations in Chinese patients with TGFBI gene-linked corneal dystrophy.

Authors:  Yan Long; Yang-Shun Gu; Wei Han; Xiu-Yi Li; Ping Yu; Ming Qi
Journal:  J Zhejiang Univ Sci B       Date:  2011-04       Impact factor: 3.066

4.  Rapid genotyping for most common TGFBI mutations with real-time polymerase chain reaction.

Authors:  Shigeo Yoshida; Yoko Yamaji; Ayako Yoshida; Yoshihiro Noda; Yuji Kumano; Tatsuro Ishibashi
Journal:  Hum Genet       Date:  2005-03-03       Impact factor: 4.132

5.  Differential expression and processing of transforming growth factor beta induced protein (TGFBIp) in the normal human cornea during postnatal development and aging.

Authors:  Henrik Karring; Kasper Runager; Zuzana Valnickova; Ida B Thøgersen; Torben Møller-Pedersen; Gordon K Klintworth; Jan J Enghild
Journal:  Exp Eye Res       Date:  2009-09-26       Impact factor: 3.467

6.  A novel variant of combined granular-lattice corneal dystrophy associated with the Met619Lys mutation in the TGFBI gene.

Authors:  Anthony J Aldave; Vivek S Yellore; Baris Sonmez; Nirit Bourla; Andrew K Salem; M Ali Khan; Sylvia A Rayner; Ben J Glasgow
Journal:  Arch Ophthalmol       Date:  2008-03

7.  Development of a Transgenic Mouse with R124H Human TGFBI Mutation Associated with Granular Corneal Dystrophy Type 2.

Authors:  Katsuya Yamazoe; Satoru Yoshida; Miyuki Yasuda; Shin Hatou; Emi Inagaki; Yoko Ogawa; Kazuo Tsubota; Shigeto Shimmura
Journal:  PLoS One       Date:  2015-07-21       Impact factor: 3.240

8.  Effect of Light Scattering and Higher-order Aberrations on Visual Performance in Eyes with Granular Corneal Dystrophy.

Authors:  Kazutaka Kamiya; Hidenaga Kobashi; Akihito Igarashi; Nobuyuki Shoji; Kimiya Shimizu
Journal:  Sci Rep       Date:  2016-04-18       Impact factor: 4.379

9.  Reduced penetrance in familial Avellino corneal dystrophy associated with TGFBI mutations.

Authors:  Wenping Cao; Hongyan Ge; Xiaobo Cui; Lu Zhang; Jing Bai; Songbin Fu; Ping Liu
Journal:  Mol Vis       Date:  2009-01-14       Impact factor: 2.367

10.  Double mutation (R124H, N544S) of TGFBI in two sisters with combined expression of Avellino and lattice corneal dystrophies.

Authors:  Naoyuki Yamada; Koji Kawamoto; Naoyuki Morishige; Tai-ichiro Chikama; Teruo Nishida; Mitsuaki Nishioka; Naoko Okayama; Yuji Hinoda
Journal:  Mol Vis       Date:  2009-05-15       Impact factor: 2.367

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