The frequency of limb girdle muscular dystrophy 2A in northeastern Italy

被引:65
作者
Fanin, M
Nascimbeni, AC
Fulizio, L
Angelini, C
机构
[1] Venetian Inst Mol Med, I-35129 Padua, Italy
[2] Univ Padua, Dept Neurosci, Padua, Italy
关键词
limb-girdle muscular dystrophy; LGMD2A; calpain-3; genetic epidemiology;
D O I
10.1016/j.nmd.2004.11.003
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Limb-girdle muscular dystrophy 2A (LGMD2A) is considered to be the most frequent LGMD. Our study surveyed an area in northeastern Italy where an almost complete ascertainment was possible. To identify LGMD2A patients we used a new diagnostic approach, including several molecular and biochemical methods. In 84 screened patients from northeastern Italy, we identified 39 LGMD2A patients, the prevalence of LGMD2A being 9.47 per million. In the Venezia district it appears higher than in other districts of the Veneto region, and in the Friuli region it is three times higher than in Veneto, due to the recurrence of single mutation. Haplotype analysis suggested a founder effect. The population from Venezia and Friuli has a higher risk of being heterozygote for these two mutant alleles than people from the rest of northeastern Italy. Our results indicate that LGMD2A is one of the most frequent autosomal recessive disorders, thus finding its molecular characterization becoming increasingly important. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:218 / 224
页数:7
相关论文
共 26 条
[21]   Calpainopathy - A survey of mutations and polymorphisms [J].
Richard, I ;
Roudaut, C ;
Saenz, A ;
Pogue, R ;
Grimbergen, JEMA ;
Anderson, LVB ;
Beley, C ;
Cobo, AM ;
de Diego, C ;
Eymard, B ;
Gallano, P ;
Ginjaar, HB ;
Lasa, A ;
Pollitt, C ;
Topaloglu, H ;
Urtizberea, JA ;
de Visser, M ;
van der Kooi, A ;
Bushby, K ;
Bakker, E ;
de Munain, AL ;
Fardeau, M ;
Beckmann, JS .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 64 (06) :1524-1540
[22]  
Richard I, 1997, AM J HUM GENET, V60, P1128
[23]   MUTATIONS IN THE PROTEOLYTIC-ENZYME CALPAIN-3 CAUSE LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE-2A [J].
RICHARD, I ;
BROUX, O ;
ALLAMAND, V ;
FOUGEROUSSE, F ;
CHIANNILKULCHAI, N ;
BOURG, N ;
BRENGUIER, L ;
DEVAUD, C ;
PASTURAUD, P ;
ROUDAUT, C ;
HILLAIRE, D ;
PASSOSBUENO, MR ;
ZATZ, M ;
TISCHFIELD, JA ;
FARDEAU, M ;
JACKSON, CE ;
COHEN, D ;
BECKMANN, JS .
CELL, 1995, 81 (01) :27-40
[24]   Normal calpain expression in genetically confirmed limb-girdle muscular dystrophy type 2A [J].
Talim, B ;
Ognibene, A ;
Mattioli, E ;
Richard, I ;
Anderson, LVB ;
Merlini, L .
NEUROLOGY, 2001, 56 (05) :692-693
[25]   Limb-girdle muscular dystrophy in Guipuzcoa (Basque Country, Spain) [J].
Urtasun, M ;
Sáenz, A ;
Roudaut, C ;
Poza, JJ ;
Urtizberea, JA ;
Cobo, AM ;
Richard, I ;
Bragado, FG ;
Leturcq, F ;
Kaplan, JC ;
Massó, JFM ;
Beckmann, JS ;
de Munain, AL .
BRAIN, 1998, 121 :1735-1747
[26]   Limb-girdle muscular dystrophy: one gene with different phenotypes, one phenotype with different genes [J].
Zatz, M ;
Vainzof, M ;
Passos-Bueno, MR .
CURRENT OPINION IN NEUROLOGY, 2000, 13 (05) :511-517