Dyslexia case study of a university student
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Abstract
A case study of developmental dyslexia of a university student is presented. The purpose of this work is to describe the process of evaluation, intervention and monitoring from the University Service of Psychological and Psychopedagogical Attention (SAP). The results indicate the importance of the development of a program adapted to individual needs and the adequate training of certain skills for learning in higher education.
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References
Asociación Americana de Psiquiatría (2013). Manual diagnóstico y estadístico de los trastornos mentales. DSM-5. Barcelona: Masson.
Astrom, R. L., Wadsworth, S. J., Olson, R. K., Willcutt, E. G., & DeFries, J. C. (2012). Genetic and enviromental etiologies of reading difficulties: DeFries-fulker analysis of reading performance data from twin pairs and their non-twins siblings. Learning and Individual Differences, 22, 365-369.
http://dx.doi.org/10.1016/j.lindif.2012.01.011
PMid:22927712 PMCid:PMC3423974
Auzias, M. (1977). Pruebas de Lateralidad. Recuperado de http://psicologia-psicopedagogia.es.tl/prueba-de-lateralidad--usual.htm
Bowers, P. G., & Wolf, M. (1993). Theoretical links among naming speed, precise timing mechanisms, and orthographic skill in dislexia. Reading and Writing: An Interdisciplinary Journal, 5, 69-85.
http://dx.doi.org/10.1007/BF01026919
Cardon, L. E., Smith, S. D., Fulker, D. W., Kimberling, W. J., Pennington, B. F., & DeFries, J. C. (1994). Quantitative trait locus for reading disability chromosome 6. Science, 266, 276-279.
http://dx.doi.org/10.1126/science.7939663
PMid:7939663
Cardon, L. E., Smith, S. D., Fulker, D. W., Kimberling, W. J., Pennington, B. F., & DeFries, J. C. (1995). Quantitative trait locus for reading disability: Correction. Science, 268, 1553.
http://dx.doi.org/10.1126/science.7777847
Costa, P.T., & McCrae, R.R. (1999). Inventario de Personalidad NEO Revisado (NEO PI-R) e InventarioNEO Reducido de Cinco Factores (NEO FFI). Madrid: TEA Ediciones.
Cuetos, F., Rodríguez, B., Ruano, E. y Arribas, D. (2007). Prolec-R, Batería de evaluación de los procesos lectores, Revisada. Madrid: TEA.
Derogatis, L. R. (1983). SCL-90-R: Administration, scoring and procedures: Manual II Towson, MD Clinical Psychometric Research.
Eden, G.F., Vanmeter, J.W., Rumsey, J.W., & Zeffiro T.A. (1996). The visual déficit theory of developmental dyslexia. NeuroImage, 4, S108-S117.
http://dx.doi.org/10.1006/nimg.1996.0061
PMid:9345535
Evans, C. E., Mellor-Clark, J., Margison, F., Barkham, M., Audin, K., Connell, J., & McGrath, G. (2000). CORE: Clinical outcomer in routine evaluation. Journal of Mental Health, 9, 247–255.
http://dx.doi.org/10.1080/jmh.9.3.247.255
http://dx.doi.org/10.1080/713680250
Fawcett, A.J., Nicolson, R. I., & Dean, P. (1996). Impaired performance of children with dyslexia on a range of cerebellar tasks. Annals of Dyslexia, 46, 259-283.
http://dx.doi.org/10.1007/BF02648179
PMid:24234275
Fisher, S. E., Marlow, A. J., Lamb, J., Mestrini, E., Williams, D. F., & Richardson, A. J. (1999). A quantitative-trait locus on chromosome 6p influencies different aspects of developmental dyslexia. American Journal of Human Genetics, 64, 146-156.
http://dx.doi.org/10.1086/302190
PMid:9915953 PMCid:PMC1377712
Fletcher, J. M. (2009). The evolution of a scientific concept. Journal of the International Neuropsychological Society, 15, 501-508.
http://dx.doi.org/10.1017/S1355617709090900
PMid:19573267 PMCid:PMC3079378
Francks, C., Fisher, S. E., Olson, R. K., Pennington, B. F., Smith, S. D., DeFries, J. C., Monaco, A. (2002). Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: Quantitative association analysisand positional candidate genes SEMA4F and OTX1. Phychiatrics Genetics, 12, 35-41.
http://dx.doi.org/10.1097/00041444-200203000-00005
Frith, U. (1997). Brain, mind and behaviour in dyslexia. En C. Hulme & M. Snowling (Eds.) Dyslexia, Biology, Cognition and Intervention. London: Whurr Publishers Ltd.
Frith, U. (1999). Paradoxes in the definition of dyslexia. Dyslexia, 5, 192-214.
http://dx.doi.org/10.1002/(SICI)1099-0909(199912)5:4<192::AID-DYS144>3.3.CO;2-E
http://dx.doi.org/10.1002/(SICI)1099-0909(199912)5:4<192::AID-DYS144>3.0.CO;2-N
Galaburda, A.M, & Livingstone, M. (1993). Evidence for a magnocellular defect in developmental dislexia. Annals of the New York Academy of Science, 682, 70-82.
http://dx.doi.org/10.1111/j.1749-6632.1993.tb22960.x
Galaburda, A. M., LoTurco, J., Ramus, F., Fitch, R. H., & Rosen, G. D. (2006). From genes to behaviour in developmental dyslexia. Nature Neuroscience, 9, 1213-1217.
http://dx.doi.org/10.1038/nn1772
PMid:17001339
Galaburda, A., Rosen, G., & Sherman, (1990). Individual variability in cortical organizations: Its reslationship to brain laterality and implications to function. Neuropsychologia, 28, 529-546.
http://dx.doi.org/10.1016/0028-3932(90)90032-J
Gayán, J., Smith, S. D., Cherny, S. S., Cardon, R. L., Fulker, D. W., Kimberling, W. J., Pennington, B. F. (1999). Quantitative-trait locus for specific language and reading deficits on chromosome 6p. American Journal of Human Genetics, (64), 157-164.
http://dx.doi.org/10.1086/302191
PMid:9915954 PMCid:PMC1377713
Gayán, J., Smith, S. D., Cherny, S. S., Cardon, R. L., Fulker, D. W., Kimberling, W. J., DeFries, J. C. (1999). Quantitative-trait locus for specific languaje and reading deficits on chromosome 6p. American Journal of Human Genetics, 64, 157-164.
http://dx.doi.org/10.1086/302191
PMid:9915954 PMCid:PMC1377713
González, D., Jiménez, J. E., García, E., Díaz, A., Rodríguez, C., & Crespo, P. (2010). Prevalencia de las dificultades específicas de aprendizaje en la ense-anza secundaria obligatoria. Europe’s Journal of Pychology, 3, 317-327.
Grigorenko, E. L., Wood, F. B., Meyer, M. S., Hart, L. A., Speed, W. C., Shuster, A., & Pauls, D. L. (1997). Susceptibility loci for distinct components of developmental dyslexia on chromosome 6 and 15. American Journal of Human Genetics, 30, 27-39.
Grigorenko, E. L., Wood, F. B., Meyer, M. S., Pauls, J. E., Hart, L. A., & Pauls, D. L. (2001). Linkage studies suggest a possible locus for developmental dyslexia on chromosome 1p. American Journal of Medical Genetics, 41, 43-49.
http://dx.doi.org/10.1002/1096-8628(20010108)105:1<120::aid-ajmg1075>3.0.co;2-t
http://dx.doi.org/10.1002/1096-8628(20010108)105:1<120::aid-ajmg1075>3.3.co;2-k
Hoien, T. (1999). Theories of déficits in dislexia. En I. Lundberg, F.E. Tonnesen & I. Austad (Eds). Dyslexia: Advances in theory and practise. London: Kluwer Academic Publishers.
Illingworth, S., & Bishop, D. V. (2009). Atypical cerebral lateralisation in adults with compensated developmental dyslexia demonstrated using functional transcranial doppler ultrasound. Brain Language, 111, 61-65.
http://dx.doi.org/10.1016/j.bandl.2009.05.002
PMid:19525003 PMCid:PMC2977530
Jiménez, J. E., Gúzman, R., Rodríguez, C., & Artiles, C. (2009). Prevalencia de las dificultades específicas de aprendizaje: La dislexia en espa-ol. Annals of Psychology, 25, 78-85.
Kaminen, N., Hannula- Jouppi, K., Kestilä, M., Lahermo, P., Muller, K., & Kaarenen, M. (2002). A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32. Journal of Medical Genetics, 40, 340-345.
http://dx.doi.org/10.1136/jmg.40.5.340
PMCid:PMC1735449
Lehongre, K., Morillon, B., Giraud, A., & Ramus, F. (2013). Impaired auditory sapling in dyslexia: Futher evidence from cobinated fMRI and EEG. Frontiers in Human Neuroscience, 7, 454.
http://dx.doi.org/10.3389/fnhum.2013.00454
PMid:23950742 PMCid:PMC3738857
Leiner, H.C., Leiner, A.L., & Dow, R.S. (1989). Reappraising the cerebellum; What does the hindbrain contribute to the forebrain? Behavioral Neuroscience, 103, 998-1008.
http://dx.doi.org/10.1037/0735-7044.103.5.998
PMid:2679667
Matute, E.; Rosselli, M., Ardila, A., y Ostrosky, F. (2007b). Evaluación Neuropsicológica Infantil. ENI. México: Manual moderno.
Mody, M. (2003). Phonological basis in Reading disability; A review and analysis of the evidence. Reading and Writing: An Interdisciplinart Journal, 16, 21-39.
http://dx.doi.org/10.1023/A:1021741921815
Nicolson, R.I., Fawcett, A.J., & Dean. P. (2001). Developmental dyslexia: the cerebellar déficit hypothesis. Trends in Neurosciences, 24 (9), 508-511.
http://dx.doi.org/10.1016/S0166-2236(00)01896-8
Nittrouer, S. (1999). Do temporal processing déficits cause phonological processing problems?. Journal of Speech, Language, and Hearing Research, 42, 925-942.
http://dx.doi.org/10.1044/jslhr.4204.925
Penninton, B. F. (1999). Toward an integrated understanding of dyslexia : Genic, neurological, and cognitive mechanisms. Development and Psychopathology, 11, 629-654.
http://dx.doi.org/10.1017/S0954579499002242
Peterson, R. L., & Penninton, B. F. (2007). Developmental dyslexia. Lancet, 379, 1997-2007.
http://dx.doi.org/10.1016/S0140-6736(12)60198-6
Petryshen, R., Kaplan, B. J., Hughes, M. L., Tzenova, J., & Field, L. L. (2002). Supportive evidence for the DYX3 dyslexia susceptibility gene in canadian families. Journal of Medical Genetics, 39, 125-126.
http://dx.doi.org/10.1136/jmg.39.2.125
PMid:11836362 PMCid:PMC1735047
Rabin, M., Wen, X. L., Hepburn, M., Lubs, H. A., Feldman, E., & Duara, R. (1993). Suggestive linkage of developmental dyslexia to chromosome 1p34-p36. Lancet, 40, 751-758.
http://dx.doi.org/10.1016/0140-6736(93)91384-x
Ramus, F., Pidgeon, E., & Frith, U. (2003). The relationship between motor control and phonology in dyslexic childen. Journal of Child Psychology and Psychiatry, 44(5), 712-722.
http://dx.doi.org/10.1111/1469-7610.00157
PMid:12831115
Serrano, F. (2005). Dislexicos en espa-ol. papel de la fonología y la ortografía (Universidad de Granada). Doi:84-338-3573-4.
Serrano, F., & Defior, S. (2008). Dyslexia speed problems in a transparent orthography. Annals of Dyslexia, 58, 81-95.
http://dx.doi.org/10.1007/s11881-008-0013-6
PMid:18483868
Skottum, B.C. (1997). The magnocellular déficit theory of dyslexia. Trends in Neuroscience, 20, 397-398.
Skottum, B.C. (2000). The magnocellular déficit theory of dyslexia: the evidence from contrast sensitivity. Vision research, 40, 111-127.
http://dx.doi.org/10.1016/S0042-6989(99)00170-4
Soriano-Ferrer, M., & Piedra Martínez, E. (2014). Una revisión de las bases neurobiológicas de la dislexia en población adulta. El Servier, (662), 8/8/2014
http://dx.doi.org/10.1016/j.nrl.2014.08.003
Spielberger C.D., Gorsuch, R.L., & Lushene, R.E. (1982). Cuestionario de Ansiedad Estado/Rasgo. Madrid: TEA.
Steinbrink, C., Groth, K., Lachmann, T., & Riecker, A. (2012). Neural correlates of temporal auditory processing in developmental dyslexia during german vowel length discrimination: An fMRI study. Brain Language, 121, 1-11.
http://dx.doi.org/10.1016/j.bandl.2011.12.003
PMid:22377262
Tallal, P., Miller, S., Fitch, R. H. (1993). Neurobiological basis of speech: a case for the preeminence of temporal processing. Annals NY Academic Science, 682, 27-47.
http://dx.doi.org/10.1111/j.1749-6632.1993.tb22957.x
Van der Leij, A., & Van Daal, H. P. (1999). Automaticity, automatization and Dyslexia. En I. L. Kundberg, F. E. Tonnessen, & I. Austad (eds), Dyslexia: Advances in Theory and Practice (pp. 75-90). Dordrecht: Kluwer Academic Publishers.
http://dx.doi.org/10.1007/978-94-011-4667-8_6
Vidal-Abarca, E, (2007). TEC. Test de estrategias de comprensión. Madrid: Instituto Calasanz de ciencias de la educación.
http://dx.doi.org/10.1021/es0706899
Wadsworth, S. J., Olson, R. K., & DeFries, J. C. (2010). Differential genetic etiology of reading difficulties as a function of IQ: An update. Behavior Genetics, 40, 751-758.
http://dx.doi.org/10.1007/s10519-010-9349-x
PMid:20333543 PMCid:PMC2892633
Wechsler, D. (1999). WAIS-III. Escala de inteligencia de Wechsler para adultos-III. Madrid, TEA (Edición original, 1997).
Wolf, M. (1991). Naming speed and Reading: The contribution of the cognitive neurosciences. Reading Research Quarterly, 26(2), 123-141.
http://dx.doi.org/10.2307/747978
Wolf, M., & Bowers, P. G. (2000). Naming Speed Processes and Developmental Reading Disabilities: An Introduction to the Special Issue on the Double-Deficit Hypothesis. Journal of Learning disabilities, 33 (4), 322-324.