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WHAT IS ATAXIA?

ATAXIA is due to a number of related neurological disorders, causing slow progressive deterioration of nerve cells in the spinal cord and cerebellum (part of the brain controlling balance). Brain and peripheral nerves are frequently involved.

ATAXIA means unsteadiness, clumsiness and lack of muscular co-ordination.

ATAXIA first appears with symptoms of stumbling or drunken walk, hand inco-ordination and slurred speech.  Symptoms progress quite rapidly in some patients over a period of 10- 1 5 years, or slowly in others over a span of 20 or more years.

ATAXIA when hereditary, is due to a defective gene passed from generation to generation, either as a dominant or recessive trait.

ATAXIA when sporadic/idiopathic appears when there is no family history of the disease and it is difficult to determine the cause.

HOW MANY PEOPLE GET ATAXIA?

Ataxia is not as rare as originally thought but is not as well recognised as neurological conditions such as multiple sclerosis or muscular dystrophy with similar symptoms.  It is estimated that there are approximately 2,500 people with recessive ataxias; 800 with dominant ataxia and a some 2,000 sporadic cases.

WHAT CAUSES ATAXIA?

Although the answer has not yet been found, research is expanding rapidly and only recently various genetic traits of ataxia have been allocated to specific chromosomes.

WHAT HELP IS AVAILABLE?

As yet there is no known treatment or cure.  It is a progressive disorder and often leads the sufferers to a wheelchair.  However, many of the associated problems of ataxia can effectively be dealt with by other professionals besides your GP; for example speech therapist, physiotherapist, etc and even alternative medicines such as reflexology and aromatherapy.

VARIOUS TYPES OF ATAXIA

Friedreich's ataxia is the most commonly known which is an inherited ataxia with onset usually occurring in childhood.

Other ataxias with recessive inheritance and early onset include spastic ataxia, cerebellar ataxia and ataxia telangiectasia, to name but a few.

Late onset ataxias include cerebellar atrophy, cerebellar ataxia, spastic ataxia, cerebellar degeneration and olivopontocerebellar atrophy or degeneration together with various ataxias with names such as Marie's Holmes, etc.

Ataxia being a condition as opposed to an illness in itself often appears as a symptom in disorders like multiple sclerosis, cerebral palsy and Charcot-Marie-Tooth disease.  


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