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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>
 
{{disease|G 23.0|Hallervorden-Spatz syndrome}}
 
==Links==
 
[https://www.wikigenes.org/e/mesh/e/9516.html wikigenes:Hallervorden-Spatz Syndrome]
 
 
[[Lewy body]]
 
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892321/pdf/BCN-7-165.pdf Case Report: Hallervorden–Spatz Syndrome with Seizures]
 
[http://www.ijaweb.org/temp/IndianJAnaesth59143-5623069_153710.pdf Sinha R, Biyani G, Bhattacharjee S. Anaesthetic management of a child with panthothenate kinase-associated neurodegeneration. Indian J Anaesth 2015;59:43-6.]
 
[http://www.scielo.br/pdf/anp/v74n5/0004-282X-anp-74-05-0423.pdf What’s in a name? Problems, facts and controversies regarding neurological eponyms]
 
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307362/pdf/ijcn-8-001.pdf Neurodegeneration with Brain Iron Accumulation: An Overview]
 
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4317075/pdf/PAMJ-19-62.pdf Maladie d’Hallervorden-Spatz chez un adulte jeune]
 
<references/>
 
[[nl:Syndroom van Hallervorden-Spatz]]
[[nl:Syndroom van Hallervorden-Spatz]]
{{Wikidata|Q1436162 read Panthothenate kinase-associated neurodegeration}}
[[Category:Disease]]

Latest revision as of 20:26, 20 June 2017