How does Spinocerebellar Ataxia affect the other organ systems?

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I'm doing a disease project and I'm a bit lost. I'm searching for all the organ systems that SCA would affect and what it does to each system. I've got nervous and muscle-- if im wrong, please correct me. Are there any other systems that are affected?
Ataxia with Identified Genetic and Biochemical Defects
Last Updated: January 19, 2007 Email to a Colleague

Synonyms and related keywords: abetalipoproteinemia, Angelman syndrome, arginase, argininemia, argininosuccinate lyase, argininosuccinate synthetase, argininosuccinic acidemia, ataxia telangiectasia, ataxia with selective vitamin E deficiency, ataxia with oculomotor apraxia, AOA, autosomal dominant ataxias, autosomal recessive ataxia, biotinidase deficiency, carbamyl phosphate synthetase deficiency, CPS deficiency, congenital disorders of glycosylation syndrome, cerebrotendinous xanthomatosis, Cockayne syndrome, CBS, Dandy Walker syndrome, defects of mitochondrial beta oxidation, dentatorubropallidoluysian atrophy, DRPLA, episodic ataxia type 1, EA1, episodic ataxia type 2, EA2, fragile X–associated tremor/ataxia syndrome, FXTAS, Friedreich's ataxia, Friedreich ataxia, GM2 gangliosidosis, Gaucher type III, Hartnup's disease, Hartnup disease, hypobetalipoproteinemia, Krabbe's globoid cell leukodystrophy, L-2 hydroxyglutaric acidemia, Lafora bodydisease, late infantile and juvenile sphingolipidoses, late infantile neuronal ceroid lipofuscinosis, late-onset urea cycle defects, Leigh's disease, Leigh disease, leukoencephalopathy with vanishing white matter, leukoencephalopathy with VWM, maple syrup urine disease, metabolic ataxias, metachromatic leukodystrophy, mitochondrial cytopathies, myoclonic epilepsy with ragged red fibers, MERRF, NARP syndrome, neuropathy ataxia retinitis pigmentosa, Niemann-Pick C disease, ornithine transcarbamylase deficiency, OTC deficiency, recessively inherited metabolic ataxias, Refsum's disease, Refsum disease, progressive myoclonic epilepsies, pyruvate dehydrogenase deficiency, pyruvate carboxylase deficiency, spinocerebellar ataxias, succinic-semialdehyde dehydrogenase deficiency, urea cycle defects, Unverricht-Lundborg disease, xeroderma pigmentosum, XP, metabolic disorder  (+ info)

Any history of patients diagnosed with Spinocerebellar ataxia recovered?

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Is there any history of patients diagnosed with Spinocerebellar ataxia ever recovered?
no there is no one who can recovered from spinocerebellar ataxia there is no cure  (+ info)

is there a known cause or cure for spinocerebellar ataxia?

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and also, if a person is diagnosed with spinocerebellar ataxia, how long are they expected to live? thanx!
In most cases the cause is hereditary and dominant. For now there are no cures for the different SCA's, but there are treatments for the symptoms. Life expectancy is usually not affected but quality of life is.

Hi,

My name is Michel Beaudet, I'm 47, have FA and live in Quebec, Canada.
I'm sending this message to invite people to join a list for those with ataxia. The list is called Internaf and
there's also a website full of info at http://internaf.org

International Network of Ataxia Friends is a mailing list for ataxia patients and family which serves as a support group and information exchange vehicle. There are currently over 680 subscribers from more than 40 countries worldwide.
Subscriptions to INTERNAF is free.
For info on how to subscribe, go see, http://internaf.org/network/services.html or
for email only access click here and send: [email protected] or
for full yahoogroups features access go to http://groups.yahoo.com/group/internaf/join

Bye
ps: Don't hesitate to email me if you have questions about internaf
--
Michel Beaudet
[email protected]
[email protected]
[email protected]
Internaf - INTERnational Network of Ataxia Friends
http://pages.infinit.net/macmike
http://groups.yahoo.com/group/internaf
http://www.internaf.org  (+ info)

Is there a cure for spinocerebellar degeneration disease?

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10 points for the best answer!!
no, there isn't.  (+ info)

What is the cause of spinocerebellar ataxia?

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or is it still unknown?
They are all genetic. There are at least 26 types, but they all involve some sort of gene mutation. The specific type of ataxia, its clinical manifestations, and its mode of inheritance depends on the gene involved. If you have a specific spinocerebellar ataxia in mind, you should Google it.

All the general information you need can be found here:
http://en.wikipedia.org/wiki/Spinocerebellar_ataxia

This is more detailed and clinical:
http://emedicine.medscape.com/article/1153370-overview

Let me know if you have any questions about a specific SCA.  (+ info)

Does anyone know what happens when you give someone with Spinocerebellar Ataxia weed?

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My dad suffers from it am Im really trying to find a way to make him better, calm his shakings and be able to hold a real conversation with him...

I smoke, and I heard about people with ataxia smoking and it helping them out, does anyone know if this has truth?

They are both against me smoking so I want to know if this is true before I bring it up with them
so ive heard...i heard in people with SCA Marijuana kills pain by activating a set of proteins known as cannabinoid receptors...

i did a bit of research heres some of the important information i have found, links provided-----

Laura J. (41) of Tennessee, was diagnosed with episodic ataxia, a rare form of spino-cerebellar ataxia (SCA). Confined to a wheelchair, she also suffers from imbalance, dizziness, blurred vision, nausea, and muscle spasms. After 20 years without a diagnosis and trying almost every medicine available with no relief, Laura switched to a complete diet rich in vitamins and cannabis. Since she had began self-medication with cannabis, her pain and spasms have dissipated, her nausea is suppressed, and she is beginning to be able to walk again. http://www.benefitsofmarijuana.com/testimonials.php


"My mother, who at age 50 resides in a nursing home, suffers from a disease known Spinocerebellar Degeneration/Axatia, and Type II diabetes. Axatia is best explained, "Persons with spinocerebellar ataxia experience a degeneration of the spinal cord and the cerebellum, the small fissured mass at the base of the brain, behind the brain stem......." "......To protect my mother, rid her of pain, and help many other patients that live with this disease and others, I believe medicinal marijuana should be legalized.
The main chemical in marijuana is delta-9-tetrahydrocannabinol or THC for short. This chemical reacts with cannaboid receptors in the human brain, which is what makes the user feel high. Certain cannaboid receptors called CB2 block pain signals being sent to human sensory nerves. As far as it is known, using marijuana is the only way to activate these cannaboid receptors" http://aleesamason.deviantart.com/art/Medicinal-Marijuana-100629008




I would seriously concider this a method of relief for your father, i am a stong beliver in the legalization of marijuana for medicinal purposes.

http://www.youtube.com/watch?v=DTWZ7W5w48s

i hope you find your father some relief, my best wishes.  (+ info)

I am taking nortriptyline to calm my sciatic neves caused by degenerations , is it safe to take procera pills?

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Nortriptyline is prescription pill and procera is otc for alziehmer.
It depends on an amount of Nortriptyline your are taking daily. Nortriptyline pills could be from 10 mg to 100 mg. And Nortriptyline by itself has pretty high cardiac toxicity. So I would advice to take extra precautions, especially if your daily dosage of Nortriptyline is more than 50 mg.

http://www.tensionheadache.medgrip.com/video  (+ info)

Is there any proper teatment or other alterations for the rare disease Spinocerebellar Ataxia 4?

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Spinocerebellar ataxia (SCA) is a progressive, degenerative genetic disease.
The condition is considered to be irreversible.
people who begin to show symptoms and are later diagnosed with spinocerebellar ataxia, a careful evaluation by a neurologist is usually required.
Fulltime caretaker and nursing support will be required in the later stages of the disease. Psychological counseling is often needed.
There is also no treatment to slow the progression of the disease.
people with spinocerebellar ataxias are encouraged to remain as active as possible.
Occupational Therapy may be helpful.
Speech therapy . often help as the person loses his or her ability to speak.  (+ info)

spinocerebellar atrophy is the same as spinocerebellar ataxia?

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I am doing a research article for my class and was doing research on the topic spinocerebellar atrophy, but when I was, it would always direct me to spinocerebellar ataxia? Are they the same thing? Does spinocerebellar atrophy lead to spinocerebellar ataxia? Help asap!!
Yes they are the same. Cerebellar atrophy leads to ataxia.  (+ info)

did doctors find cure for the spinocerebellar degeneration disease?

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Sarah Jean,
In brief, not yet. Most disorders that result in ataxia, which is a neurological sign and symptom consisting of gross lack of coordination of muscle movements, cause cells in the part of the brain called the cerebellum to degenerate, or atrophy. Sometimes the spine is also affected. The phrases cerebellar degeneration and spinocerebellar degeneration are used to describe changes that have taken place in a person’s nervous system; neither term constitutes a specific diagnosis. Cerebellar and spinocerebellar degeneration have many different causes. The age of onset of the resulting ataxia varies depending on the underlying cause of the degeneration. Many ataxias are hereditary and are classified by chromosomal location and pattern of inheritance: autosomal dominant, in which the affected person inherits a normal gene from one parent and a faulty gene from the other parent; and autosomal recessive, in which both parents pass on a copy of the faulty gene. Among the more common inherited ataxias are Friedreich’s ataxia and Machado-Joseph disease. Sporadic ataxias can also occur in families with no prior history. There is no cure for the hereditary ataxias. If the ataxia is caused by another condition, that underlying condition is treated first. For example, ataxia caused by a metabolic disorder may be treated with medications and a controlled diet. Vitamin deficiency is treated with vitamin therapy. A variety of drugs may be used to treat gait and swallowing disorders. Physical therapy can strengthen muscles, while special devices or appliances can assist in walking and other activities of daily life. The prognosis for individuals with ataxia and cerebellar/spinocerebellar degeneration varies depending on its underlying cause.

ALL ANSWERS SHOULD BE THOROUGHLY RESEARCHED, IN ANY FORUM AND ESPECIALLY IN THIS ONE. - MANY ANSWERS ARE FLAWED.

It is extremely important to obtain an accurate diagnosis before trying to find a cure. Many diseases and conditions share common symptoms.


The information provided here should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions.


I add a link with details of this subject


http://www.dizziness-and-balance.com/
disorders/central/cerebellar/sca.htm


Hope this helps
matador 89  (+ info)

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