How does Spinocerebellar Ataxia affect the other organ systems? - what systems does tendonitis affect
I'm doing a project of the disease and I am a bit lost. I'm happy for all organs and systems, the SCA and does affect every system. I'm nervous and muscular - if I'm wrong, please correct me please. Are there other systems that are affected?
Thursday, February 4, 2010
What Systems Does Tendonitis Affect How Does Spinocerebellar Ataxia Affect The Other Organ Systems?
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Ataxia recognized genetic and biochemical changes
Last updated: January 19, 2007 via e-mail 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, ataxia, autosomal dominant, autosomal Recessive ataxia, biotinidase deficiency, a deficiency of carbamyl phosphate synthetase, 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's ataxia, GM2 gangliosidosis, Gaucher type III, Hartnup disease, Hartnup disease, hypobetalipoproteinemia, Krabbe globoid leukodystrophy-L-2 hydroxyglutaric acidemia, Bo Laforadydis Sphingolipidoses late infantile and juvenile, late infantile neuronal ceroid lipofuscinosis late-onset urea cycle defects, Leigh syndrome, Leigh disease, theft of white matter disease, leukoencephalopathy with VWM leukoencephalopathy, maple syrup urine metabolic ataxia, metachromatic leukodystrophy, mitochondrial disorders, myoclonic epilepsy with ragged red fibers syndrome, MERRF, NARP, neuropathy, ataxia, retinitis pigmentosa, Niemann-Pick C, ornithine transcarbamylase deficiency, OTC deficiency, ataxia recessive hereditary metabolic disease Refsum disease Refsum, progressive myoclonus epilepsy, pyruvate dehydrogenase , pyruvate carboxylase deficiency, spinocerebellar ataxia, succinic semialdehyde dehydrogenase, malformations of the urea cycle, Unverricht Lundborg disease, xeroderma pigmentosum, XP, metabolic
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