From genes to behavior in developmental dyslexia

被引:240
作者
Galaburda, Albert M.
LoTurco, Joseph
Ramus, Franck
Fitch, R. Holly
Rosen, Glenn D.
机构
[1] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Neurol,Div Behav Neurol, Boston, MA 02215 USA
[2] Univ Connecticut, Dept Physiol & Neurobiol, Storrs, CT 06269 USA
[3] Ecole Normale Super, Lab Sci Cognit & Psycholinguist, F-75230 Paris 05, France
[4] Univ Connecticut, Dept Psychol Behav Neurosci, Storrs, CT 06269 USA
关键词
D O I
10.1038/nn1772
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
All four genes thus far linked to developmental dyslexia participate in brain development, and abnormalities in brain development are increasingly reported in dyslexia. Comparable abnormalities induced in young rodent brains cause auditory and cognitive deficits, underscoring the potential relevance of these brain changes to dyslexia. Our perspective on dyslexia is that some of the brain changes cause phonological processing abnormalities as well as auditory processing abnormalities; the latter, we speculate, resolve in a proportion of individuals during development, but contribute early on to the phonological disorder in dyslexia. Thus, we propose a tentative pathway between a genetic effect, developmental brain changes, and perceptual and cognitive deficits associated with dyslexia.
引用
收藏
页码:1213 / 1217
页数:5
相关论文
共 48 条
[1]   A YAC contig in xq22.3-q23, from DXS287 to DXS8088, spanning the brain-specific genes doublecortin (DCX) and PAK3 [J].
Allen, KM ;
Gleeson, JG ;
Shoup, SM ;
Walsh, CA .
GENOMICS, 1998, 52 (02) :214-218
[2]   Developmental dyslexia and specific language impairment: Same or different? [J].
Bishop, DVM ;
Snowling, MJ .
PSYCHOLOGICAL BULLETIN, 2004, 130 (06) :858-886
[3]  
Butterworth B., 2005, Handbook of mathematical cognition, P455
[4]   QUANTITATIVE TRAIT LOCUS FOR READING-DISABILITY ON CHROMOSOME-6 [J].
CARDON, LR ;
SMITH, SD ;
FULKER, DW ;
KIMBERLING, WJ ;
PENNINGTON, BF ;
DEFRIES, JC .
SCIENCE, 1994, 266 (5183) :276-279
[5]   Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia [J].
Chang, BS ;
Appignani, B ;
Bodell, A ;
Apse, KA ;
Ravenscroft, RS ;
Sheen, VL ;
Doherty, MJ ;
Hackney, DB ;
O'Connor, M ;
Galaburda, AM ;
Walsh, CA .
NEUROLOGY, 2005, 64 (05) :799-803
[6]   Linkage analyses of four regions previously implicated in dyslexia: Confirmation of a locus on chromosome 15q [J].
Chapman, NH ;
Igo, RP ;
Thomson, JB ;
Matsushita, M ;
Brkanac, Z ;
Holzman, T ;
Berninger, VW ;
Wijsman, EM ;
Raskind, WH .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2004, 131B (01) :67-75
[7]   Impaired two-tone processing at rapid rates in male rats with induced microgyria [J].
Clark, MG ;
Rosen, GD ;
Tallal, P ;
Fitch, RH .
BRAIN RESEARCH, 2000, 871 (01) :94-97
[8]   Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia [J].
Cope, N ;
Harold, D ;
Hill, G ;
Moskvina, V ;
Stevenson, J ;
Holmans, P ;
Owen, MJ ;
O'Donovan, MC ;
Williams, J .
AMERICAN JOURNAL OF HUMAN GENETICS, 2005, 76 (04) :581-591
[9]   Common and divergent roles for members of the mouse DCX superfamily [J].
Coquelle, Frederic M. ;
Levy, Talia ;
Bergmann, Sven ;
Wolf, Sharon Grayer ;
Bar-El, Daniela ;
Sapir, Tamar ;
Brody, Yehuda ;
Orr, Irit ;
Barkai, Naama ;
Eichele, Gregor ;
Reiner, Orly .
CELL CYCLE, 2006, 5 (09) :976-983
[10]   SPATIAL-LEARNING, DISCRIMINATION-LEARNING, PAW PREFERENCE AND NEOCORTICAL ECTOPIAS IN 2 AUTOIMMUNE STRAINS OF MICE [J].
DENENBERG, VH ;
SHERMAN, GF ;
SCHROTT, LM ;
ROSEN, GD ;
GALABURDA, AM .
BRAIN RESEARCH, 1991, 562 (01) :98-104