3 AUTOSOMAL-DOMINANT CORNEAL DYSTROPHIES MAP TO CHROMOSOME-5Q

被引:137
作者
STONE, EM
MATHERS, WD
ROSENWASSER, GOD
HOLLAND, EJ
FOLBERG, R
KRACHMER, JH
NICHOLS, BE
GOREVIC, PD
TAYLOR, CM
STREB, LM
FISHBAUGH, JA
DALEY, TE
SUCHESKI, BM
SHEFFIELD, VC
机构
[1] UNIV IOWA, COLL MED, DEPT PATHOL, IOWA CITY, IA 52242 USA
[2] UNIV IOWA, COLL MED, DEPT PEDIAT, IOWA CITY, IA 52242 USA
[3] PENN STATE UNIV, MILTON S HERSHEY MED CTR, COLL MED, DEPT OPHTHALMOL, HERSHEY, PA 17033 USA
[4] UNIV MINNESOTA, COLL MED, DEPT OPHTHALMOL, MINNEAPOLIS, MN 55455 USA
[5] SUNY STONY BROOK, DIV RHEUMATOL & CLIN IMMUNOL, STONY BROOK, NY 11794 USA
关键词
D O I
10.1038/ng0194-47
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The two most common autosomal dominant dystrophies of the corneal stroma are lattice corneal dystrophy type I and granular dystrophy. A third autosomal dominant stromal dystrophy (Avellino) has also been recognized. Chromosome linkage analysis of four families with Avellino dystrophy mapped the disease-causing gene to chromosome 5q. Subsequent linkage analysis of two families with typical lattice dystrophy and two with typical granular dystrophy also revealed significant linkage with the same markers. Thus, each of three clinically and histopathologically distinct phenotypes is independently linked to 5q. The maximum combined lod score using all 114 affected patients was 28.6 with marker D5S393. None of the 14 known human amyloid-associated genes map to chromosome 5.
引用
收藏
页码:47 / 51
页数:5
相关论文
共 32 条
  • [1] FAST AND SENSITIVE SILVER STAINING OF DNA IN POLYACRYLAMIDE GELS
    BASSAM, BJ
    CAETANOANOLLES, G
    GRESSHOFF, PM
    [J]. ANALYTICAL BIOCHEMISTRY, 1991, 196 (01) : 80 - 83
  • [2] HEREDITARY RENAL AMYLOIDOSIS ASSOCIATED WITH A MUTANT FIBRINOGEN ALPHA-CHAIN
    BENSON, MD
    LIEPNIEKS, J
    UEMICHI, T
    WHEELER, G
    CORREA, R
    [J]. NATURE GENETICS, 1993, 3 (03) : 252 - 255
  • [3] GELSOLIN-DERIVED FAMILIAL AMYLOIDOSIS CAUSED BY ASPARAGINE OR TYROSINE SUBSTITUTION FOR ASPARTIC-ACID AT RESIDUE 187
    DELACHAPELLE, A
    TOLVANEN, R
    BOYSEN, G
    SANTAVY, J
    BLEEKERWAGEMAKERS, L
    MAURY, CPJ
    KERE, J
    [J]. NATURE GENETICS, 1992, 2 (02) : 157 - 160
  • [4] DWELET FE, 1984, P NATN ACAD SCI USJO, V81, P694
  • [5] FOLBERG R, 1988, OPHTHALMOLOGY, V95, P46
  • [6] HEREDITARY CEREBRAL AMYLOID ANGIOPATHY - THE AMYLOID FIBRILS CONTAIN A PROTEIN WHICH IS A VARIANT OF CYSTATIN-C, AN INHIBITOR OF LYSOSOMAL CYSTEINE PROTEASES
    GHISO, J
    PONSESTEL, B
    FRANGIONE, B
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1986, 136 (02) : 548 - 554
  • [7] SEGREGATION OF A MISSENSE MUTATION IN THE AMYLOID PRECURSOR PROTEIN GENE WITH FAMILIAL ALZHEIMERS-DISEASE
    GOATE, A
    CHARTIERHARLIN, MC
    MULLAN, M
    BROWN, J
    CRAWFORD, F
    FIDANI, L
    GIUFFRA, L
    HAYNES, A
    IRVING, N
    JAMES, L
    MANT, R
    NEWTON, P
    ROOKE, K
    ROQUES, P
    TALBOT, C
    PERICAKVANCE, M
    ROSES, A
    WILLIAMSON, R
    ROSSOR, M
    OWEN, M
    HARDY, J
    [J]. NATURE, 1991, 349 (6311) : 704 - 706
  • [8] POLYMERIZATION OF INTACT BETA-2-MICROGLOBULIN IN TISSUE CAUSES AMYLOIDOSIS IN PATIENTS ON CHRONIC-HEMODIALYSIS
    GOREVIC, PD
    MUNOZ, PC
    CASEY, TT
    DIRAIMONDO, CR
    STONE, WJ
    PRELLI, FC
    RODRIGUES, MM
    POULIK, MD
    FRANGIONE, B
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (20) : 7908 - 7912
  • [9] A SIMPLE AND EFFICIENT NON-ORGANIC PROCEDURE FOR THE ISOLATION OF GENOMIC DNA FROM BLOOD
    GRIMBERG, J
    NAWOSCHIK, S
    BELLUSCIO, L
    MCKEE, R
    TURCK, A
    EISENBERG, A
    [J]. NUCLEIC ACIDS RESEARCH, 1989, 17 (20) : 8390 - 8390
  • [10] HOLLAND EJ, 1992, OPHTHALMOLOGY, V99, P1564