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Hallervorden-Spatz syndrome: Difference between revisions
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[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892321/pdf/BCN-7-165.pdf Case Report: Hallervorden–Spatz Syndrome with Seizures] | [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892321/pdf/BCN-7-165.pdf Case Report: Hallervorden–Spatz Syndrome with Seizures] | ||
[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] | |||
<references/> | <references/> |
Revision as of 19:22, 20 June 2017
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
Case Report: Hallervorden–Spatz Syndrome with Seizures
What’s in a name? Problems, facts and controversies regarding neurological eponyms
read Panthothenate kinase-associated neurodegeration Interwiki via Wikidata