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Hallervorden-Spatz syndrome: Difference between revisions

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Hallervorden-Spatz syndrome, now known as pantothenate kinase-associated neurodegeneration (PKAN), is an autosomal recessive disorder causing involuntary spasticity and progressive dementia <ref>http://radiopaedia.org/articles/hallervorden-spatz-syndrome</ref>
Hallervorden-Spatz syndrome, now known as pantothenate kinase-associated neurodegeneration (PKAN), is an autosomal recessive disorder causing involuntary spasticity and progressive dementia <ref>http://radiopaedia.org/articles/hallervorden-spatz-syndrome</ref>
{{disease|G 23.0}}
 
{{disease|G 23.0|Hallervorden-Spatz syndrome}}
 
==Links==
==Links==
[https://www.wikigenes.org/e/mesh/e/9516.html wikigenes:Hallervorden-Spatz Syndrome]
[https://www.wikigenes.org/e/mesh/e/9516.html wikigenes:Hallervorden-Spatz Syndrome]


<references/>
<references/>
[[nl:Syndroom van Hallervorden-Spatz]]
[[nl:Syndroom van Hallervorden-Spatz]]

Revision as of 04:38, 13 September 2015

Hallervorden-Spatz syndrome, now known as pantothenate kinase-associated neurodegeneration (PKAN), is an autosomal recessive disorder causing involuntary spasticity and progressive dementia [1]

Disease classification WHO
G 23.0 Hallervorden-Spatz syndrome

Links

wikigenes:Hallervorden-Spatz Syndrome