Literature DB >> 23949389

Putative miRNAs for the diagnosis of dyslexia, dyspraxia, and specific language impairment.

Alexander Rudov1, Marco Bruno Luigi Rocchi1, Augusto Accorsi1, Giorgio Spada2, Antonio Domenico Procopio3, Fabiola Olivieri3, Maria Rita Rippo3, Maria Cristina Albertini1.   

Abstract

Disorders of human communication abilities can be classified into speech and language disorders. Speech disorders (e.g., dyspraxia) affect the sound generation and sequencing, while language disorders (e.g., dyslexia and specific language impairment, or SLI) are deficits in the encoding and decoding of language according to its rules (reading, spelling, grammar). The diagnosis of such disorders is often complicated, especially when a patient presents more than one disorder at the same time. The present review focuses on these challenges. We have combined data available from the literature with an in silico approach in an attempt to identify putative miRNAs that may have a key role in dyspraxia, dyslexia and SLI. We suggest the use of new miRNAs, which could have an important impact on the three diseases. Further, we relate those miRNAs to the axon guidance pathway and discuss possible interactions and the role of likely deregulated proteins. In addition, we describe potential differences in expressional deregulation and its role in the improvement of diagnosis. We encourage experimental investigations to test the data obtained in silico.

Entities:  

Keywords:  SLI; dyslexia; dyspraxia; in silico analysis; miRNA

Mesh:

Substances:

Year:  2013        PMID: 23949389      PMCID: PMC3891682          DOI: 10.4161/epi.26026

Source DB:  PubMed          Journal:  Epigenetics        ISSN: 1559-2294            Impact factor:   4.528


  42 in total

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  2 in total

Review 1.  MicroRNAs and Child Neuropsychiatric Disorders: A Brief Review.

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2.  Neuroimaging genetic associations between SEMA6D, brain structure, and reading skills.

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  2 in total

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