Template:Central nervous system disease: Difference between revisions

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| group2 = Systemic [[atrophies]]<BR>primarily affecting the CNS
| group2 = Systemic [[atrophies]]<BR>primarily affecting the CNS
| list2 = [[Huntington's disease]] - [[Spinocerebellar ataxia]] ([[Friedreich's ataxia]], [[Ataxia telangiectasia]], [[Hereditary spastic paraplegia]]) - [[Spinal muscular atrophy]]: [[Werdnig-Hoffman disease|Werdnig-Hoffman]] - [[Kugelberg-Welander disease|Kugelberg-Welander]] - [[Fazio Londe syndrome|Fazio Londe]] - [[Motor neurone disease|MND]] ([[Amyotrophic lateral sclerosis|ALS]], [[Progressive muscular atrophy|PMA]], [[Progressive bulbar palsy|PBP]], [[Pseudobulbar palsy|PP]], [[Primary lateral sclerosis|PLS]])
| list2 = [[Huntington's disease]] - [[Spinocerebellar ataxia]] ([[Friedreich's ataxia]], [[Ataxia telangiectasia]], [[Hereditary spastic paraplegia]]) - [[Spinal muscular atrophy]]: [[Werdnig-Hoffman disease|Werdnig-Hoffman]] - [[Kugelberg-Welander disease|Kugelberg-Welander]] - [[Fazio-Londe disease|Fazio-Londe]] - [[Motor neurone disease|MND]] ([[Amyotrophic lateral sclerosis|ALS]], [[Progressive muscular atrophy|PMA]], [[Progressive bulbar palsy|PBP]], [[Pseudobulbar palsy|PP]], [[Primary lateral sclerosis|PLS]])


| group3 = [[Extrapyramidal]] and<BR>[[movement disorder]]s
| group3 = [[Extrapyramidal]] and<BR>[[movement disorder]]s

Revision as of 08:31, 6 July 2008