Lectura y escritura en niños con síndrome X frágil: Estrategias de intervención

Ma Paz Fernández-Lozano, Aníbal Puente-Ferreras, Ma Teresa Ferrando-Lucas

Resultado de la investigación: Article

2 Citas (Scopus)

Resumen

Syndrome X fragile (SXF) is the most common cause of inhe-rited intellectual disability. It's characterized by a very specific physical and behavioral phenotype. The SXF is caused by a mutation in the FMR1 gene located on chromosome X, locus Xq27.3. Gene mutation causes an abnormal number of repetitions of the triple CGG (cytosine-guanine-guanine). The SXF analysis represents a good model to determine the relationship between genes and behavior. The area of reading and writing in the fragile X population samples too many dark areas. The main problems of the SXF with reading and writing have their origin in disorders of language and motor difficulties and sensory integration. Our work aims to expand and systematize organically some aspects that we consider fundamental for improving educational practice and restore reading deficiencies. In this line of action we highlight both methodological strategies and programmed proposals which should be explored to learn about their educational value and practical effectiveness.

Idioma originalSpanish
Páginas (desde-hasta)808-815
Número de páginas8
PublicaciónAnales de Psicologia
Volumen27
N.º3
EstadoPublished - 2011

Huella dactilar

Fragile X Syndrome
Reading
Guanine
Genes
Language Disorders
Mutation
Cytosine
X Chromosome
Intellectual Disability
Phenotype
Population

ASJC Scopus subject areas

  • Psychology(all)

Citar esto

Fernández-Lozano, Ma Paz ; Puente-Ferreras, Aníbal ; Ferrando-Lucas, Ma Teresa. / Lectura y escritura en niños con síndrome X frágil : Estrategias de intervención. En: Anales de Psicologia. 2011 ; Vol. 27, N.º 3. pp. 808-815.
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abstract = "Syndrome X fragile (SXF) is the most common cause of inhe-rited intellectual disability. It's characterized by a very specific physical and behavioral phenotype. The SXF is caused by a mutation in the FMR1 gene located on chromosome X, locus Xq27.3. Gene mutation causes an abnormal number of repetitions of the triple CGG (cytosine-guanine-guanine). The SXF analysis represents a good model to determine the relationship between genes and behavior. The area of reading and writing in the fragile X population samples too many dark areas. The main problems of the SXF with reading and writing have their origin in disorders of language and motor difficulties and sensory integration. Our work aims to expand and systematize organically some aspects that we consider fundamental for improving educational practice and restore reading deficiencies. In this line of action we highlight both methodological strategies and programmed proposals which should be explored to learn about their educational value and practical effectiveness.",
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Fernández-Lozano, MP, Puente-Ferreras, A & Ferrando-Lucas, MT 2011, 'Lectura y escritura en niños con síndrome X frágil: Estrategias de intervención', Anales de Psicologia, vol. 27, n.º 3, pp. 808-815.

Lectura y escritura en niños con síndrome X frágil : Estrategias de intervención. / Fernández-Lozano, Ma Paz; Puente-Ferreras, Aníbal; Ferrando-Lucas, Ma Teresa.

En: Anales de Psicologia, Vol. 27, N.º 3, 2011, p. 808-815.

Resultado de la investigación: Article

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T1 - Lectura y escritura en niños con síndrome X frágil

T2 - Estrategias de intervención

AU - Fernández-Lozano, Ma Paz

AU - Puente-Ferreras, Aníbal

AU - Ferrando-Lucas, Ma Teresa

PY - 2011

Y1 - 2011

N2 - Syndrome X fragile (SXF) is the most common cause of inhe-rited intellectual disability. It's characterized by a very specific physical and behavioral phenotype. The SXF is caused by a mutation in the FMR1 gene located on chromosome X, locus Xq27.3. Gene mutation causes an abnormal number of repetitions of the triple CGG (cytosine-guanine-guanine). The SXF analysis represents a good model to determine the relationship between genes and behavior. The area of reading and writing in the fragile X population samples too many dark areas. The main problems of the SXF with reading and writing have their origin in disorders of language and motor difficulties and sensory integration. Our work aims to expand and systematize organically some aspects that we consider fundamental for improving educational practice and restore reading deficiencies. In this line of action we highlight both methodological strategies and programmed proposals which should be explored to learn about their educational value and practical effectiveness.

AB - Syndrome X fragile (SXF) is the most common cause of inhe-rited intellectual disability. It's characterized by a very specific physical and behavioral phenotype. The SXF is caused by a mutation in the FMR1 gene located on chromosome X, locus Xq27.3. Gene mutation causes an abnormal number of repetitions of the triple CGG (cytosine-guanine-guanine). The SXF analysis represents a good model to determine the relationship between genes and behavior. The area of reading and writing in the fragile X population samples too many dark areas. The main problems of the SXF with reading and writing have their origin in disorders of language and motor difficulties and sensory integration. Our work aims to expand and systematize organically some aspects that we consider fundamental for improving educational practice and restore reading deficiencies. In this line of action we highlight both methodological strategies and programmed proposals which should be explored to learn about their educational value and practical effectiveness.

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KW - Read

KW - Strategies

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KW - Write

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