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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><references/> | 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> | ||
==Links== | |||
[https://www.wikigenes.org/e/mesh/e/9516.html wikigenes:Hallervorden-Spatz Syndrome] | |||
<references/> | |||
[[nl:Syndroom van Hallervorden-Spatz]] | [[nl:Syndroom van Hallervorden-Spatz]] | ||
Revision as of 04:26, 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]