Guanine to adenine mutations in patients with lattice corneal dystrophy

被引:3
作者
El-Shabrawi, Y [1 ]
Ardjomand, N
Faschinger, C
Höfler, G
机构
[1] Graz Univ, Augenklin, A-8036 Graz, Austria
[2] Anat Pathol Inst Graz, Graz, Austria
来源
OPHTHALMOLOGE | 1999年 / 96卷 / 06期
关键词
lattice dystrophy; cornea; beta ig-h3-mutation-kerato-epitheline gene;
D O I
10.1007/s003470050426
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Background: Lattice dystrophy is an autosomal-dominantly inherited disease. A mutation of the gene coding for kerato-epitheline has been found in patients with this stromal dystrophy. In codon 124 a Guanine to Adenine mutation of the nucleotide 417 has been described. We looked for this mutation in a family with lattice dystrophy treated in our clinic. Patients and methods: Using primers specific for kerato-epitheline gene, we amplified the cDNA extracted from lymphocytes of two patients suffering from lattice dystrophy. The polymerase chain reaction (PCR) products were subcloned and sequenced. Results: Guanine to Adenine mutations, as published were detected in both of our patients at codon 124. Conclusion: We found the published mutation in both of our patients, indicating that this Guanine to Adenine exchange is pathognomonic for lattice dystrophy.
引用
收藏
页码:405 / 407
页数:3
相关论文
共 15 条
[1]   CORNEAL CELL MATRIX INTERACTIONS - TYPE-VI COLLAGEN PROMOTES ADHESION AND SPREADING OF CORNEAL FIBROBLASTS [J].
DOANE, KJ ;
YANG, G ;
BIRK, DE .
EXPERIMENTAL CELL RESEARCH, 1992, 200 (02) :490-499
[2]  
El-Shabrawi Y, 1998, INVEST OPHTH VIS SCI, V39, P36
[3]   CDNA FROM HUMAN OCULAR CILIARY EPITHELIUM HOMOLOGOUS TO BETA-IG-H3 IS PREFERENTIALLY EXPRESSED AS AN EXTRACELLULAR PROTEIN IN THE CORNEAL EPITHELIUM [J].
ESCRIBANO, J ;
HERNANDO, N ;
GHOSH, S ;
CRABB, J ;
COCAPRADOS, M .
JOURNAL OF CELLULAR PHYSIOLOGY, 1994, 160 (03) :511-521
[4]   Lattice corneal dystrophy type 1 in a Canadian kindred is associated with the Arg124 → Cys mutation in the kerato-epithelin gene [J].
Gupta, SK ;
Hodge, WG ;
Damji, KF ;
Guernsey, DL ;
Neumann, PE .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1998, 125 (04) :547-549
[5]  
Holbach LM, 1997, PATHOLOGIE AUGES, P507
[6]   BETA-IG-H3, A NOVEL SECRETORY PROTEIN INDUCIBLE BY TRANSFORMING GROWTH-FACTOR-BETA, IS PRESENT IN NORMAL SKIN AND PROMOTES THE ADHESION AND SPREADING OF DERMAL FIBROBLASTS IN-VITRO [J].
LEBARON, RG ;
BEZVERKOV, KI ;
ZIMBER, MP ;
PAVELEC, R ;
SKONIER, J ;
PURCHIO, AF .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1995, 104 (05) :844-849
[7]   Lattice corneal dystrophy type I. Clinical and molecular genetic analysis in a large family [J].
Meins, M ;
Kohlhaas, M ;
Richard, G ;
Gal, A .
KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, 1998, 212 (03) :154-158
[8]   Kerato-epithelin mutations in four 5q31-linked corneal dystrophies [J].
Munier, FL ;
Korvatska, E ;
Djemai, A ;
LePaslier, D ;
Zografos, L ;
Pescia, G ;
Schorderet, DF .
NATURE GENETICS, 1997, 15 (03) :247-251
[9]  
Okada M, 1998, INVEST OPHTH VIS SCI, V39, P1947
[10]  
Rawe IM, 1997, INVEST OPHTH VIS SCI, V38, P893