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There are several thousand children who suffer learning
disability (LD) such as dyslexia, dyscalculia, and attention
deficit hyperactivity disorder (ADHD), processing disorders
and nonverbal and suspect LD. Research has shown that these
underachievers seldom get the right opportunity to come out
of their disability.
Learning disabilities (LD) are neurobiological in nature.
How do we know this? Over the last decade, particularly,
compelling scientific evidence from genetic research and
studies of the brain has clearly demonstrated the
neurobiological basis of learning disabilities.
Genetic Link to Learning Disabilities
A genetic basis for learning disabilities has been confirmed
through twin studies, sibling analysis and family pedigree
analysis. Twin studies have shown that if one twin has a
reading disability, the probability of the other twin also
having a reading disability is 68 per cent for identical
twins (monozygotic) and 40 per cent for fraternal twins (dizygotic).
Familial transmission of LD has been investigated, and has
shown that if there is a family history (parents, siblings,
and extended family) of reading disabilities, the
probability of having a reading disability is significantly
increased. Several modes of transmission have been
investigated. Although there are, as yet, no definitive
conclusions, a possible linkage to chromosomes 6 and 15 has
been identified.
Early Development of the Brain
Fetal brain development is complex; cells grow, multiply,
migrate, and establish interconnections and a communication
system. Growth continues over a prolonged period of time,
and the first three years of brain development are critical.
Cells in the early stage reproduce at an astonishing rate of
250,000 a minute. The human brain has approximately 100
billion neurons and one trillion glial cells (supporting
cells). The cells assemble themselves in a series of tightly
choreographed steps, with clockwork precision. The cells
migrate to distant locations. Wiring the brain involves
trillions of connections between neurons linking one part of
the brain to another. The developing brain undergoes an
incredible metamorphosis through a series of extraordinary
changes.
Nature is the dominant factor driving this phase of
development, but nurture plays a vital role. Changes in the
environment can interfere with the precision of development.
Sensory experiences contribute to shaping, thereby
determining which connections develop and which ones are
pruned. Normal growth can be disrupted by a wide variety of
factors. Environmental events, such as toxin exposure, can
significantly alter outcome. Early development as well as
later cognitive and behavioural development can be affected.
Negative effects on brain development include: prenatal
factors; toxic and teratogenic agents; poor nutrition; very
low birth weight; gestational age; oxygen deprivation; early
oxygen dependence; neonatal seizures; hemorrhages;
resistance to thyroid hormones; PCBs and other dioxins;
alcohol, cigarettes, marijuana, and cocaine; lead and
cadmium; and iron and chloride deficiencies.
Measuring the Brain
A variety of methods are now available to measure the
physical structure as well as the function of the brain.
Neuroanatomical techniques include autopsy studies; neuro-imaging
techniques include CT scan, MRI, PET, rCBF, and SPECT;
electrophysiological measures include EEG, ERP, and AEP; and
neuropsychological assessments evaluate brain/behaviour
relationships.
A number of studies of brain structure and function have
been carried out on subjects with LD. One method to look at
structural differences in the brain is through the
microscope in postmortem or autopsy studies. Postmortem
findings have indicated that the normal brain has
asymmetries. For example, one side of the brain is not
exactly the same as the other. These asymmetries are
expected and considered normal (just as it is quite ordinary
or typical for one foot to be longer than the other).
Important research efforts have focused on reading
disabilities, since they represent the most common and
frequently identified type of LD. Studies have shown that
brains of subjects with reading disabilities have no
asymmetry in brain structures where there should be
asymmetry, that is, there is an absence of ordinary
asymmetry. For example, the temporal lobe (planum temporale
area) in the left hemisphere has been found to be typically
larger than the temporal lobe (planum temporale area) in the
right hemisphere in subjects without LD (asymmetrical),
whereas, this area in the left hemisphere has been found to
be the same size as in the right hemisphere in subjects with
LD.
Another technique for studying the brain is the CT scan
(computed tomography (roentgen-ray)) With this technique, a
beam of x-rays is shot through the brain, identifying bone,
grey matter, and fluid. A computer then reconstructs an
image of each slice or brain section, allowing abnormalities
in structure to be detected. CT scans of the occipital lobe,
for example, have shown asymmetry of the occipital pole in
subjects without LD and symmetry in subjects with LD.
Magnetic resonance imaging (MRI) is a technique that
involves picking up the electromagnetic energy of brain
protons and constructing an image by superimposing magnetic
fields. MRI research has shown that subjects without LD
showed leftward asymmetry in the angular gyrus of the
parietal lobe, whereas subjects with LD did not show the
expected asymmetry.
It has been demonstrated through autopsy, CT Scan, and MRI
studies, that there are structural differences in the brains
of subjects with LD in comparison to subjects without LD. It
has also been demonstrated that there are differences in
brain function in the subjects with LD, that is, how the
brain works. Functional neuroimaging techniques, including
PET (positron emission tomography), rCBF (regional cerebral
blood flow), fMRI (functional magnetic resonance imaging),
and SPECT (single photon emission computed tomography), are
used to measure brain activity while subjects are engaged in
a task such as reading. An fMRI is a non-invasive method
that measures blood flow, while PET and SPECT methods
involve the injection of radioactive materials. SPECT scan
results have indicated that subjects with LD show
underfunctioning in the occipital lobe while reading, in
comparison to subjects without LD.
Electroencephalograms (EEGs), event related potentials (ERPs),
and averaged evoked potentials (AEPs) record electrical
activity of the brain through electrodes. Research has shown
that subjects with LD (dyslexia) showed less electrical
activity in the parietal lobe, in comparison to subjects
without LD.
Neuropsychological assessments include a variety of tests of
cognitive/intellectual, language, visual-perceptual,
academic, motor, sensory, and emotional/behavioural
abilities and functions. A profile of strengths and
weaknesses is then correlated with known brain functions.
The neuropsychological research has indicated significant
findings as well. Deficiencies in language/verbal learning,
reading, written language, verbal reasoning, verbal memory,
arithmetic computation, and processing speed have been
associated with left hemispheric dysfunction. Deficiencies
in spatial function, nonverbal reasoning, nonverbal cues,
social skills, and social/emotional information have been
associated with right hemispheric dysfunction. Phonological
processing deficits have been identified as a primary
difficulty in subjects with language and reading
disabilities, and structural and functional abnormalities in
the medial geniculate nuclei have been associated with these
findings.
Through the application of these investigative procedures,
anomalies in brain structure and associated dysfunction have
been implicated in subjects with LD. Some of these include:
the planum temporale, medial geniculate nuclei, perisylvian
regions, frontal cortex, parietal operculum, inferior
parietal lobe, temporal gyrus, corpus callosum, insular
region, angular gyrus, occipital-striatal region, and the
brainstem reticular activating system.
Conclusion and Implications
There is significant scientific evidence from genetic
research and studies of the brain that has demonstrated the
neurobiological basis of learning disabilities. There are
differences in both brain structure and brain function, and
these findings have important implications. Educators must
recognize and accept the scientific evidence, establish
policies, develop effective educational programs, and match
the instructional goals, content, and pace of teaching
specifically to the learning needs of individuals with LD so
that these individuals can achieve maximum success.
It is important to emphasize that individuals with LD can
learn, but the process may be inefficient as a result of the
specific differences in brain structure and function.
Inefficiency refers to either low accuracy or low speed in
learning or performing a task and is quite distinct from
inability or incapacity. Information can be processed, but
at a slower rate and/or by different methods as compared to
individuals without LD. The educational process, learning
strategies, compensatory techniques, and remedial
intervention can significantly impact the learning process.
Therefore, effective and efficient learning and teaching
methods are needed to specifically meet the needs of
individuals with LD.
The conference is intended to produce a blueprint of action
to help governments and educational institutions design
curriculum, evolve interventional methods and build up
training resources to address the problems of
under-achievers. We offer opportunities to the delegates to
interact with specialists, initiate dialogue and network in
order to harness the current knowledge and practices in this
field.
The conference is a path breaking initiative that would
throw up several techniques, procedures and training
programmes designed to meet the learning styles and
educational needs of the intellectually challenged. Experts
in the fields of clinical psychology, neuro sciences,
government, research, education, corporate and parents
will debate and explore ways to address the problems of
children with learning disabilities.
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