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Article

HARP syndrome is allelic with pantothenate kinase-associated neurodegeneration.

Neurology - 11 Jun 2002

Ching K H L, Westaway S K, Gitschier J, Higgins J J, Hayflick S J

Abstract excerpt

HARP (hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration) is a rare syndrome with many clinical similarities to pantothenate kinase-associated neurodegeneration (PKAN, formerly Hallervorden-Spatz syndrome). Despite these common features, lipoprotein abnormalities have not been reported in PKAN. After the recent discovery of the genetic defect in PKAN, we report a...

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Source

Identifiers

PMID: 12058097
DOI: 10.1212/wnl.58.11.1673

Genes

PANK2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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