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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/PMC4317075/pdf/PAMJ-19-62.pdf Maladie d’Hallervorden-Spatz chez un adulte jeune]


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Revision as of 20:08, 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

Sinha R, Biyani G, Bhattacharjee S. Anaesthetic management of a child with panthothenate kinase-associated neurodegeneration. Indian J Anaesth 2015;59:43-6.

What’s in a name? Problems, facts and controversies regarding neurological eponyms


Maladie d’Hallervorden-Spatz chez un adulte jeune

  1. ↑ http://radiopaedia.org/articles/hallervorden-spatz-syndrome

Q1436162 read Panthothenate kinase-associated neurodegeration at Wikidata  read Panthothenate kinase-associated neurodegeration Interwiki via Wikidata

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