The genetic bases of speech sound disorders: Evidence from spoken and written language

被引:55
作者
Lewis, Barbara A.
Shriberg, Lawrence D.
Freebairn, Lisa A.
Hansen, Amy J.
Stein, Catherine M.
Taylor, H. Gerry
Iyengar, Sudha K.
机构
[1] Case Western Reserve Univ, Cleveland, OH 44106 USA
[2] Univ Wisconsin, Waisman Res Ctr, Madison, WI 53706 USA
来源
JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH | 2006年 / 49卷 / 06期
关键词
genetics; reading disorders; speech sound disorders; language disorders;
D O I
10.1044/1092-4388(2006/093)
中图分类号
R36 [病理学]; R76 [耳鼻咽喉科学];
学科分类号
100104 ; 100213 ;
摘要
The purpose of this article is to review recent findings suggesting a genetic susceptibility for speech sound disorders (SSD), the most prevalent communication disorder in early childhood. The importance of genetic studies of SSD and the hypothetical underpinnings of these genetic findings are reviewed, as well as genetic associations of SSD with other language and reading disabilities. The authors propose that many genes contribute to SSD. They further hypothesize that some genes contribute to SSD disorders alone, whereas other genes influence both SSD and other written and spoken language disorders. The authors postulate that underlying common cognitive traits, or endophenotypes, are responsible for shared genetic influences of spoken and written language. They review findings from their genetic linkage study and from the literature to illustrate recent developments in this area. Finally, they discuss challenges for identifying genetic influence on SSD and propose a conceptual framework for study of the genetic basis of SSD.
引用
收藏
页码:1294 / 1312
页数:19
相关论文
共 150 条
[1]  
[Anonymous], EXPRESSIVE 1 WORD PI
[2]  
[Anonymous], TEST WRITTEN SPELLIN
[3]  
ARAM DM, 1989, SCHOOL PSYCHOL REV, V18, P487
[4]  
BAKWIN H, 1973, DEV MED CHILD NEUROL, V15, P184
[5]   Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment [J].
Bartlett, CW ;
Flax, JF ;
Logue, MW ;
Smith, BJ ;
Vieland, VJ ;
Tallal, P ;
Brzustowicz, LM .
HUMAN HEREDITY, 2004, 57 (01) :10-20
[6]   A major susceptibility locus for specific language impairment is located on 13q21 [J].
Bartlett, CW ;
Flax, JF ;
Logue, MW ;
Vieland, VJ ;
Bassett, AS ;
Tallal, P ;
Brzustowicz, LM .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (01) :45-55
[7]   Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia [J].
Belton, E ;
Salmond, CH ;
Watkins, KE ;
Vargha-Khadem, F ;
Gadian, DG .
HUMAN BRAIN MAPPING, 2003, 18 (03) :194-200
[8]  
BENNINGTON BF, 1991, J CHILD PSYCHOL PSYC, V31, P193
[9]  
BISGAARD ML, 1987, CLIN GENET, V32, P118
[10]   Developmental dyslexia and specific language impairment: Same or different? [J].
Bishop, DVM ;
Snowling, MJ .
PSYCHOLOGICAL BULLETIN, 2004, 130 (06) :858-886