The FRAXopathies: Definition, Overview, and Update

被引:31
作者
Pirozzi, Filomena [1 ]
Tabolacci, Elisabetta [1 ]
Neri, Giovanni [1 ]
机构
[1] Univ Cattolica, Ist Genet Med, I-00168 Rome, Italy
关键词
fragile X syndrome; FXTAS; FXPO1; FMR1; gene; pharmacological approaches; FRAGILE-X-SYNDROME; MENTAL-RETARDATION PROTEIN; METABOTROPIC GLUTAMATE-RECEPTOR; PREMATURE OVARIAN FAILURE; FMR1; MESSENGER-RNA; TREMOR/ATAXIA SYNDROME FXTAS; CGG REPEAT NUMBER; FULL-MUTATION; DROSOPHILA MODEL; DOUBLE-BLIND;
D O I
10.1002/ajmg.a.34113
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The fragile X syndrome, fragile X tremor ataxia syndrome, and premature ovarian insufficiency are conditions related to the X chromosome folate-sensitive fragile site FRAXA. Therefore, we propose that they are considered as a family of disorders under the general designation of FRAXopathies. The present review will outline the main clinical and molecular features of these disorders, with special emphasis on the pathogenic mechanisms that lead to distinct phenotypes, starting from related mutations. The understanding of these mechanisms is already generating promising therapeutic approaches. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:1803 / 1816
页数:14
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