| Autor: |
Milanlıoğlu, Aysel, Aydın, Mehmet Nuri, Gökgül, Alper, Hamamcı, Mehmet, Tombul, Temel |
| Předmět: |
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| Zdroj: |
Eastern Journal of Medicine; Oct-Dec2013, Vol. 18 Issue 4, p221-223, 3p |
| Abstrakt: |
Hallervorden-Spatz syndrome is a rare neurodegenerative disease, resulting from mutation in the Pantothenate kinase-2 gene, and characterized by progressive pyramidal and extrapyramidal dysfunction, dementia, retinal degeneration and optic nerve atrophy. Clinical symptoms are related to abnormal iron deposition in the globus pallidus and substantia nigra. We present a case report of a 50-year old woman that was diagnosed as atypical Hallervorden-Spatz disease with dominant extrapyramidal symptoms and the lack of typical eye-of-the-tiger sign in brain MRI. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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