| Literature DB >> 1443412 |
H Tsukamoto1, K Inui, M Taniike, J Nishimoto, M Midorikawa, T Yoshimine, A Kato, T Ikeda, T Hayakawa, S Okada.
Abstract
We present a 10-year-old girl with Hallervorden-Spatz disease diagnosed clinically from the neurological manifestations and the characteristic MRI findings. Her main symptom, dystonia, was progressive and resistant to medication, but this dystonia was controlled by bilateral thalamotomy. No clinical progression of the symptoms was recognized at 21 months from the last operation.Entities:
Mesh：
Year: 1992 PMID： 1443412 DOI： 10.1016/s0387-7604(12)80246-4
Source DB: PubMed Journal: Brain Dev ISSN： 0387-7604 Impact factor: 1.961