Adult-onset atypical form of Hallervorden-Spatz disease

Year 2013, Volume: 18 Issue: 4, 221 - 223, 14.03.2014

Aysel Milanlıoglu , Mehmet Nuri Aydın , Alper Gökgül Mehmet Hamamcı Temel Tombul

https://izlik.org/JA65JM55UX

Abstract

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.

Keywords

Hallervorden-Spatz disease , iron deposition , eye-of-the-tiger sign , neurodegeneration related to pantothenate kinase , basal ganglia

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