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...
Zapisane w:
| Główni autorzy: | , , , , |
|---|---|
| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
Liaquat University of Medical and Health Sciences
2022-12-01
|
| Seria: | JLUMHS |
| Hasła przedmiotowe: | |
| Dostęp online: | https://www.lumhs.edu.pk/jlumhs/Vol21No04/12.pdf |
| Etykiety: |
Nie ma etykietki, Dołącz pierwszą etykiete!
|