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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| 主要な著者: | , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Liaquat University of Medical and Health Sciences
2022-12-01
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| シリーズ: | JLUMHS |
| 主題: | |
| オンライン･アクセス: | https://www.lumhs.edu.pk/jlumhs/Vol21No04/12.pdf |
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