Literature DB >> 16352477

Meesmann corneal dystrophy (MECD): report of 2 families and a novel mutation in the cornea specific keratin 12 (KRT12) gene.

Olivia Nichini1, Violaine d'Allèves Manzi, Francis L Munier, Daniel F Schorderet.   

Abstract

PURPOSE: Meesmann corneal dystrophy (MECD) is an autosomal dominant disorder affecting the corneal epithelium. It is caused by heterozygous mutations in KRT3 or KRT12 gene. Actually, 14 mutations have been reported, 1 in KRT3 and 13 in KRT12. These genes were screened in several patients suffering from MECD.
METHODS: Patients from 2 families were screened for mutation in KRT3 and KRT12. Exons were PCR-amplified and directly sequenced. The new mutation was checked by DHPLC in 51 control individuals of Swiss origin. RESULTS/
CONCLUSIONS: In one family, the M129T heterozygous mutation was observed in KRT12. In the second family, we identified a novel I426S heterozygous mutation in exon 6 of KRT12.

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Year:  2005        PMID: 16352477     DOI: 10.1080/13816810500374391

Source DB:  PubMed          Journal:  Ophthalmic Genet        ISSN: 1381-6810            Impact factor:   1.803


  7 in total

1.  Identification of a novel mutation in the cornea specific keratin 12 gene causing Meesmann's corneal dystrophy in a German family.

Authors:  Ina Clausen; Gernot I W Duncker; Claudia Grünauer-Kloevekorn
Journal:  Mol Vis       Date:  2010-05-29       Impact factor: 2.367

Review 2.  The IC3D classification of the corneal dystrophies.

Authors:  Jayne S Weiss; H U Møller; Walter Lisch; Shigeru Kinoshita; Anthony J Aldave; Michael W Belin; Tero Kivelä; Massimo Busin; Francis L Munier; Berthold Seitz; John Sutphin; Cecilie Bredrup; Mark J Mannis; Christopher J Rapuano; Gabriel Van Rij; Eung Kweon Kim; Gordon K Klintworth
Journal:  Cornea       Date:  2008-12       Impact factor: 2.651

3.  The TGFBI R555W mutation induces a new granular corneal dystrophy type I phenotype.

Authors:  Yanan Zhu; Xingchao Shentu; Wei Wang
Journal:  Mol Vis       Date:  2011-01-20       Impact factor: 2.367

4.  Genetics of Meesmann corneal dystrophy: a novel mutation in the keratin 3 gene in an asymptomatic family suggests genotype-phenotype correlation.

Authors:  Jacek P Szaflik; Monika Ołdak; Radosław B Maksym; Anna Kamińska; Agnieszka Pollak; Monika Udziela; Rafał Płoski; Jerzy Szaflik
Journal:  Mol Vis       Date:  2008-09-15       Impact factor: 2.367

5.  Identification of presumed pathogenic KRT3 and KRT12 gene mutations associated with Meesmann corneal dystrophy.

Authors:  Judy L Chen; Benjamin R Lin; Katherine M Gee; Jessica A Gee; Duk-Won D Chung; Ricardo F Frausto; Sophie X Deng; Anthony J Aldave
Journal:  Mol Vis       Date:  2015-12-31       Impact factor: 2.367

6.  Identification of a Novel Missense KRT12 Mutation in a Vietnamese Family with Meesmann Corneal Dystrophy.

Authors:  Pham Ngoc Dong; Le Xuan Cung; Tran Khanh Sam; Do Thi Thuy Hang; Doug D Chung; Turad A Alkadi; Arjun Buckshey; Junwei Zhang; Alexa Kassels; Anthony J Aldave
Journal:  Case Rep Ophthalmol       Date:  2020-03-17

7.  A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophy.

Authors:  Lori S Sullivan; Eric B Baylin; Ramon Font; Stephen P Daiger; Jay S Pepose; Thomas E Clinch; Hisashi Nakamura; Xinping C Zhao; Richard W Yee
Journal:  Mol Vis       Date:  2007-06-21       Impact factor: 2.367

  7 in total

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