KEGG   DISEASE: 読字障害
エントリ  
H01899                                                             
名称    
読字障害
概要    
Dyslexia is defined by severe difficulties in reading acquisition, often accompanied by spelling difficulties and affects a large number of people (5-10%). It is caused by multiple genetic and environmental risk factors as well as their interplay. Several candidate genes have been identified in the past decade. However, effects of individual genetic variations on dyslexia-associated deficits are only moderate. At the brain level, dyslexia is associated with aberrant structure and function, particularly in left hemisphere reading-language networks.
カテゴリ  
精神及び行動の障害
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 21 症状, 徴候, 臨床所見, 他に分類されないもの
  神経系の症状, 徴候または臨床所見
   神経系の症状または徴候
    MB4B  表象機能の障害
     H01899  読字障害
病因遺伝子 
(DYX1) DNAAF4 [HSA:161582] [KO:K19758]
(DYX2) AAVR [HSA:9856] [KO:K24403]
リンク   
ICD-11: MB4B.0
MeSH: D004410
OMIM: 127700 600202
文献    
  著者
Peterson RL, Pennington BF
  タイトル
Developmental dyslexia.
  雑誌
Annu Rev Clin Psychol 11:283-307 (2015)
DOI:10.1146/annurev-clinpsy-032814-112842
文献    
  著者
Svensson I, Nilsson S, Wahlstrom J, Jernas M, Carlsson LM, Hjelmquist E
  タイトル
Familial dyslexia in a large Swedish family: a whole genome linkage scan.
  雑誌
Behav Genet 41:43-9 (2011)
DOI:10.1007/s10519-010-9395-4
文献    
  著者
Shastry BS
  タイトル
Developmental dyslexia: an update.
  雑誌
J Hum Genet 52:104-9 (2007)
DOI:10.1007/s10038-006-0088-z
文献    
  著者
Mannel C, Meyer L, Wilcke A, Boltze J, Kirsten H, Friederici AD
  タイトル
Working-memory endophenotype and dyslexia-associated genetic variant predict dyslexia phenotype.
  雑誌
Cortex 71:291-305 (2015)
DOI:10.1016/j.cortex.2015.06.029
文献    
PMID:12954984 (DYX1)
  著者
Taipale M, Kaminen N, Nopola-Hemmi J, Haltia T, Myllyluoma B, Lyytinen H, Muller K, Kaaranen M, Lindsberg PJ, Hannula-Jouppi K, Kere J
  タイトル
A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain.
  雑誌
Proc Natl Acad Sci U S A 100:11553-8 (2003)
DOI:10.1073/pnas.1833911100
文献    
PMID:15717286 (DYX2)
  著者
Cope N, Harold D, Hill G, Moskvina V, Stevenson J, Holmans P, Owen MJ, O'Donovan MC, Williams J
  タイトル
Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.
  雑誌
Am J Hum Genet 76:581-91 (2005)
DOI:10.1086/429131
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