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20  HANDBOOK OF ELECTRONIC ASSISTIVE TECHNOLOGY



             MULTIPLE SCLEROSIS
             In the United Kingdom and similar societies, multiple sclerosis (MS) is the commonest
             disabling, neurological problem in young adults with a prevalence of 1.2/1000.
                The exact reasons why MS happens are partly still being discovered; there is so much
             we still need to learn about the disease. Sticking it in an autoimmune section would
             cause huge grief to half the neurology community and just a transient nod from the other
             half. Many believe that there is at least partially an autoimmune element in that our own
             lymphocytes attack the myelin around nerve axons, disrupting the speed of messages.
             Over time axons and neurons deteriorate and a more progressive disease takes hold,
             with increasing spasticity and disability. There is also a variety of genetic and environ-
             mental factors.
                Episodes of subtle signs and symptoms initially resolve but over a longer period the
             clinical signs from the deficits may stay and progress. Repeated episodes occur as new
             areas of damage occur within the CNS. MRI scans show areas of demyelination of differing
             ages and stages.
                There are four types dependent on the speed  of onset and progression: relapsing–
             remitting, secondary and primary progressive and progressive–relapsing. Initial signs are
             variable but usually include sensory, visual or motor disturbance. Before the problems
             become multiple there is a group of around 30% who do not progress.
                A variety of treatment options have been tried and once again this is an area of huge
             trial resource internationally, using oral, injected or intrathecal antiinflammatory, immune
             modulating or immunosuppressive drugs or more recently using the power of restorative
             stem cells.
                Support in mobility, communication and ways to maintain independence are key in
             any individual management programme.
                Other autoimmune disorders of the CNS are found at the brain and spinal cord levels
             and once again specific patterns are associated with specific organisms. We have already
             mentioned postviral infective encephalitis, but the autoimmune encephalitides are caused
             by antibodies attacking proteins within the CNS. Examples include the increasingly recog-
             nised N-methyl-d-aspartate receptor antibodies; encephalitis, sparked off by a number of
             organisms, including herpes simplex and varicella (chicken pox) viruses; poststreptococ-
             cal syndromes such as Sydenham’s chorea; and acute disseminated encephalomyelitis, a
             severe autoimmune-inflammatory disease, rare but particularly seen in childhood.
                Systemic immune disorders such as sarcoidosis and systemic lupus erythematosus can
             also affect the CNS.
             PARKINSONISM
              •   Overall prevalence – 1.5/1000.
              •   Over age 60 prevalence – 1/100.
              •   Over age 80 prevalence – 3/100.

                At least seven genes have been implicated in the degeneration of the dopamine trans-
             mitting neurons of the basal ganglia area of the substantia nigra. This causes a chemical
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