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Hallervorden-Spatz syndrome: Difference between revisions
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[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] | [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] | [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4317075/pdf/PAMJ-19-62.pdf Maladie d’Hallervorden-Spatz chez un adulte jeune] |
Revision as of 20:11, 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
Neurodegeneration with Brain Iron Accumulation: An Overview
Maladie d’Hallervorden-Spatz chez un adulte jeune
read Panthothenate kinase-associated neurodegeration Interwiki via Wikidata