Hallervorden-Spatz Disease: Case Report based on Radiological and Genetic Analytical Findings

Hallervorden-Spatz disease is a rare disorder characterized by progressive extrapyramidal dysfunction and dementia. The disease can be familial or sporadic. PKAN is inherited recessively; it has been linked to chromosome 20. A mutation in the pantothenate kinase (PANK-2) gene has been described...

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Principais autores:	Ayesha Sardar, Muhammad Ashfaq, Bader-U-Nisa, Aijaz Ahmed, Hira Waseem
格式:	Artigo
语言:	Inglês
出版:	Liaquat University of Medical and Health Sciences 2022-12-01
丛编:	JLUMHS
主题:	dystonia hallervorden-spatz disease tiger-eye appearance movement disorder pantothenate kinase two deficiency
在线阅读:	https://www.lumhs.edu.pk/jlumhs/Vol21No04/12.pdf
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