Unfolding the genetic pathways of dyslexia in Asian population: A review
| Autor: | Rajesh Sagar, Pawan Sharma |
|---|---|
| Rok vydání: | 2017 |
| Předmět: |
0301 basic medicine
Asia Dyslexia Specific reading disorder Spell General Medicine Heritable disorder medicine.disease Genetic pathways Biological theories of dyslexia Developmental psychology 03 medical and health sciences Psychiatry and Mental health 030104 developmental biology 0302 clinical medicine mental disorders Asian population medicine Learning to read Humans Psychology 030217 neurology & neurosurgery General Psychology |
| Zdroj: | Asian Journal of Psychiatry. 30:225-229 |
| ISSN: | 1876-2018 |
| DOI: | 10.1016/j.ajp.2017.06.006 |
| Popis: | Dyslexia also known as specific reading disorder is a complex heritable disorder with unexpected difficulty in learning to read and spell despite adequate intelligence, education, environment, and normal senses. Over past decades, researchers have attempted to characterize dyslexia neurobiological and genetic levels and unfold its pathophysiology. The genetic research on dyslexia has received attention in Asia from the last decade. Though limited by different constraints the studies from Asia have been able to gather significant evidence in this field. We present a review of studies of genetics in Asian population and suggest future directions. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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