Congenital cataracts and their molecular genetics

被引:292
作者
Hejtmancik, J. Fielding [1 ]
机构
[1] NEI, MOGS, OGVFB, NIH, Bethesda, MD 20892 USA
关键词
lens; cataract; molecular genetics; gene;
D O I
10.1016/j.semcdb.2007.10.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cataract can be defined as any opacity of the crystalline lens. Congenital cataract is particularly serious because it has the potential for inhibiting visual development, resulting in permanent blindness. Inherited cataracts represent a major contribution to congenital cataracts, especially in developed countries. While cataract represents a common end stage of mutations in a potentially large number of genes acting through varied mechanisms in practice most inherited cataracts have been associated with a subgroup of genes encoding proteins of particular importance for the maintenance of lens transparency and homeostasis. The increasing availability of more detailed information about these proteins and their functions and is making it possible to understand the pathophysiology of cataracts and the biology of the lens in general. Published by Elsevier Ltd.
引用
收藏
页码:134 / 149
页数:16
相关论文
共 174 条
[1]  
Addison PKF, 2006, MOL VIS, V12, P791
[2]   A PROGRESSIVE EARLY-ONSET CATARACT GENE MAPS TO HUMAN-CHROMOSOME 17Q24 [J].
ARMITAGE, MM ;
KIVLIN, JD ;
FERRELL, RE .
NATURE GENETICS, 1995, 9 (01) :37-40
[3]   A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract:: further evidence for gap junction dysfunction in human cataract -: art. no. e2 [J].
Arora, A ;
Minogue, PJ ;
Liu, X ;
Reddy, MA ;
Ainsworth, JR ;
Bhattacharya, SS ;
Webster, AR ;
Hunt, DM ;
Ebihara, L ;
Moore, AT ;
Beyer, EC ;
Berthoud, VM .
JOURNAL OF MEDICAL GENETICS, 2006, 43 (01)
[4]   Mutations of a human homologue of the Drosophila eyes absent gene (EYA1) detected in patients with congenital cataracts and ocular anterior segment anomalies [J].
Azuma, N ;
Hirakiyama, A ;
Inoue, T ;
Asaka, A ;
Yamada, M .
HUMAN MOLECULAR GENETICS, 2000, 9 (03) :363-366
[5]   Gene conversion mutation in crystallin, β-B2 (CRYBB2) in a Chilean family with autosomal dominant cataract [J].
Bateman, J. Bronwyn ;
von-Bischhoffshaunsen, Fernando R. Barria ;
Richter, Leslie ;
Flodman, Pamela ;
Burch, Douglas ;
Spence, M. Anne .
OPHTHALMOLOGY, 2007, 114 (03) :425-432
[6]   A new locus for autosomal dominant cataract on chromosome 19: Linkage analyses and screening of candidate genes [J].
Bateman, J. Bronwyn ;
Richter, Leslie ;
Flodman, Pamela ;
Burch, Douglas ;
Brown, Sandra ;
Penrose, Philip ;
Paul, Otis ;
Geyer, David D. ;
Brooks, David G. ;
Spence, M. Anne .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2006, 47 (08) :3441-3449
[7]  
Bateman JB, 2000, INVEST OPHTH VIS SCI, V41, P3278
[8]  
Bateman JB, 2000, INVEST OPHTH VIS SCI, V41, P2665
[9]   MUTATION IN THE IRON-RESPONSIVE ELEMENT OF THE L-FERRITIN MESSENGER-RNA IN A FAMILY WITH DOMINANT HYPERFERRITINEMIA AND CATARACT [J].
BEAUMONT, C ;
LENEUVE, P ;
DEVAUX, I ;
SCOAZEC, JY ;
BERTHIER, M ;
LOISEAU, MN ;
GRANDCHAMP, B ;
BONNEAU, D .
NATURE GENETICS, 1995, 11 (04) :444-446
[10]   The lens organizes the anterior segment: Specification of neural crest cell differentiation in the avian eye [J].
Beebe, DC ;
Coats, JM .
DEVELOPMENTAL BIOLOGY, 2000, 220 (02) :424-431