Hallervorden Spatz disease (Pantothenate Kinase associated Neurodegeneration): a rare case report

  • et al.
N/ACitations
Citations of this article
6Readers
Mendeley users who have this article in their library.

Abstract

Hallervorden-Spatz disease now more commonly known as Pantothenate kinase-associated neurodegeneration (PKAN) is a rare autosomal recessive neurodegenerative disorder associated with iron accumulation in the brain nuclei and characterized by progressive extrapyramidal dysfunction and dementia.

Cite

CITATION STYLE

APA

Gupta, Dr. A., B.S., Dr. S., & Shetty, Dr. S. (2016). Hallervorden Spatz disease (Pantothenate Kinase associated Neurodegeneration): a rare case report. Pediatric Review: International Journal of Pediatric Research, 3(10), 759–762. https://doi.org/10.17511/ijpr.2016.i10.08

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free