A study into the causes of Dyslexia

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A study into the causes of Dyslexia

Any discussion of the causes of dyslexia must, as we shall see, be a complex and controversial undertaking; even the title may raise controversy: what is 'dyslexia'? Is it the same as 'specific learning difficulties'? Can it be defined as a single problem? Is there a continuum of dyslexic-type difficulties? Should we be using a label at all? The questions are many, and with very few satisfactory answers. For this reason, it is necessary to begin with a working definition of dyslexia, before discussing what may cause it. Once this has been established, it will be seen that the cited causes may be usefully grouped into several categories ( genetic, perceptual, neurological and linguistic). Each of these areas will be examined in some depth, and the evidence evaluated. It will be found that, as yet, no single cause can be definitively established, but that studies into information and language processing in the brain seem to offer the most promising possibilities for the future.

        Due to the complex nature of the problem, and the many different ways in which it manifests itself, it is impossible to find a definition upon which everyone may agree. Nevertheless, several definitions exist which may serve as a starting point. An early definition by Critchley is that dyslexia is "a disorder of children who, despite conventional classroom experience, fail to attain the language skills of reading, writing and spelling commensurate with their intellectual abilities." This raises two main points: what is 'conventional classroom experience', and how can we prove what level of language skills are 'commensurate with intellectual ability'? This definition was improved upon in 1978 by Critchley and Critchley: "children with specific learning difficulties are those who in the absence of sensory defect or overt organic damage, have an intractable learning problem in one or more of reading, spelling or maths, and who do not respond to normal teaching," (see also, Critchley and Critchley in Augur, 1981). Several issues are raised here - the label 'specific learning difficulties' is introduced, 'sensory defects' and 'organic damage' are mentioned, and dismissed, and so is 'normal teaching'. It is hoped that the issues of sensory defect and organic damage will be dealt with later, so that it shall be possible to consider whether this definition is accurate. The use of the term 'specific learning difficulties' (SpLD) is outside the scope of this essay, and so the more widely known 'dyslexia' will be used for convenience, even though its use is still controversial (Stanovich, 1994). Dyslexia covers a group of symptoms, any or all of which may be seen in one individual, and which can be briefly summarised as: visual perceptual difficulties, directional confusion, sequencing problems, short term and long term memory problems, difficulties in naming, organisational problems, and general literacy skills (Robertson, 1994).

        The question of whether dyslexia is genetically determined has a long history, going back to 1900 when Hinshelwood, Morgan and Kerr noted that with two boys they saw who were intelligent but could not read, there were several cases in each family, which lead him to suggest the term 'congenital word blindness', (see Huston, 1987). More recent research has supported the view that dyslexia runs in families, and is therefore at least partly genetically determined, for example, Dr Beve Hornsby reported that 88% of children seen by her had a family history of dyslexia (Osmond, 1993 and Hornsby,1992). However, these conclusions were based on observation rather than scientific method. Jorm (1983) quotes a study by Finucci et al (1976), who conducted a more stringent test and found that in 45% of cases, immediate family members of the dyslexic person were also retarded readers, confirming the strong tendency for dyslexia to run in families. However, it is important to consider whether one explanation for this apparent 'genetic' cause may be that those in families share the same environment i.e. if one or both parents don't read very well, then it is not unexpected that their children have difficulties. To try and clear up this confusion, we turn to twin studies, of which many have been conducted. Twin studies are important because they allow comparison between monozygotic twins (who share 100% genes) and dizygotic twins (who share 50%), but where both have been brought up in the same environment, so that any difference between dizygotic twins can be reliably concluded to be based on genes rather than environment. Using this method, Herman (1959) found a 100% concordance for monozygotic twins, and 33% for dizygotic twins: this is a summary of three studies undertaken in Scandinavia in the 1950s. Jorm (1983) states that all twin studies show greater similarity between MZ than DZ twins, suggesting a role for genetic factors. However, as Young and Tyre (1983) point out, this is not absolutely conclusive, unless we can be sure that these MZ twins have not been subject to perinatal disturbances, which are more likely than in single births. A related question is why more boys are affected than girls (the ratio is 3:1) - some researchers have suggested that dyslexia may be sex-linked genetically (for example on the X chromosome), although there appears to be little medical or scientific evidence for this as yet. A recent article in The Daily Telegraph (January 5th, 1996) quoted a study from 1994 in which an American team linked dyslexia to chromosome 6, suggesting a biological basis; future research should provide more information. The only reliable conclusion which can be drawn, is that genetics do appear to play a part in the causation of dyslexia, but they do not fully explain it: a combination of factors need to operate together for dyslexia to manifest itself. In addition, genetics offer no explanation for cases in which there is no family history of dyslexia.

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        Before one can read, it is necessary to hear the spoken word (audition), and see the written word (vision): these abilities may be grouped under the term 'perception'. Galaburda (1993) has described perception as "the gateway to cognition" i.e. we cannot think about something until we have perceived it. Faulty perception was one of the first areas of research about the causation of dyslexia: Hinshelwood used the term 'word blindness' (Bryant and Bradley, 1985), and Samuel Orton coined the term 'strephosymbolia' (Bryant and Bradley, 1985). He Has observed the directional confusion which is common in dyslexia (for example, b/d confusion, ...

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