الملخص
Hallervorden-Spatz disease (HSD) is a rare disorder characterized by progressive extrapyramidal dysfunction and dementia. Hallervorden and Spatz first described the disease, in 1922 as a form of familial brain degeneration characterized by iron deposition in the brain. Here we present four HSD cases with different clinical pictures.
الكلمات المفتاحية
الموضوع
بيانات النشر
- المعرّف الرقمي
- 10.4103/2277-9175.140623
- المجلة
- Advanced Biomedical Research, 3(1), 191
- الناشر
- Wolters Kluwer Medknow Publications
- وصول مفتوح
- وصول مفتوح ذهبي
- الترخيص
- CC BY-NC-SA 4.0
اقتبس هذه المقالة
APA 7
Dashti, M., & Chitsaz, A. (2014). Hallervorden-Spatz disease. Advanced Biomedical Research, 3(1), 191. https://doi.org/10.4103/2277-9175.140623
MLA 9
Dashti, Maseumeh, and Ahmad Chitsaz. "Hallervorden-Spatz disease." Advanced Biomedical Research, vol. 3, no. 1, 2014, pp. 191. https://doi.org/10.4103/2277-9175.140623.
شيكاغو (المؤلف–التاريخ)
Dashti, Maseumeh, and Ahmad Chitsaz. 2014. "Hallervorden-Spatz disease." Advanced Biomedical Research 3 (1): 191. https://doi.org/10.4103/2277-9175.140623.
هارفارد
Dashti, M. and Chitsaz, A. (2014) 'Hallervorden-Spatz disease', Advanced Biomedical Research, 3(1), pp. 191. doi:10.4103/2277-9175.140623.
فانكوفر
Dashti M, Chitsaz A. Hallervorden-Spatz disease. Advanced Biomedical Research. 2014;3(1):191. doi:10.4103/2277-9175.140623
IEEE
M. Dashti, and A. Chitsaz, "Hallervorden-Spatz disease," Advanced Biomedical Research, vol. 3, no. 1, pp. 191, 2014, doi: 10.4103/2277-9175.140623.