1. Pallidopyramidal Syndrome and Hereditary Spastic Paraplegia common features and diagnostic approach and therapeutic considerations
- Author
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Corneliu Angelo Bulboaca, Dana Festila, Ioana Stanescu, Mihai Blidaru, and Paul Mihai Boarescu
- Subjects
0301 basic medicine ,Pediatrics ,medicine.medical_specialty ,Hereditary spastic paraplegia ,business.industry ,lcsh:RM1-950 ,neurodegeneration ,General Medicine ,medicine.disease ,extrapyramidal syndrome ,03 medical and health sciences ,lcsh:Therapeutics. Pharmacology ,030104 developmental biology ,0302 clinical medicine ,pallidopyramidal syndrome ,Pallidopyramidal syndrome ,medicine ,hereditary spastic paraplegia ,business ,030217 neurology & neurosurgery - Abstract
The neurological diagnosis, can be, in some situations, a challenging one. Clinical presentation for neurological disease, which has no imagistic diagnosis criteria, can develop during several month or years. Therefore, the first evaluation of the patient with neurological symptoms is not always conclusive. Pallidopyramidal syndrome and hereditary spastic paraplegia (HSP) can present common features and diagnostic approach has to be careful. genetic assessment is the gold diagnosis method in some cases. Therapeutic strategies, following a correct diagnosis has to be addressed to improvement the patient's quality of life by rehabilitation methods and medication targeting the pathophysiological processes involvement. The aim of this paper is to discuss the clinical evolution and the diagnosis strategies in hereditary spastic paraplegia.
- Published
- 2019
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