[Molecular genetics study of hereditary spastic paraplegia accompanied by distal amyotrophy-an update]

Autor: Zhen-zhen, Wang, Zhi-dong, Cen, Wei, Luo
Rok vydání: 2013
Předmět:
Zdroj: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 30(4)
ISSN: 1003-9406
Popis: Hereditary spastic paraplegia(HSP or SPG) is a clinically and genetically heterogeneous group of neurodegenerative diseases characterized by progressive spasticity, weakness of lower limbs, and pathologically by retrograde axonal degeneration of corticospinal tracts and posterior spinal tracts. Presence of additional features allows differentiation between simple and complex forms of the disease. Genetically, 16 loci for HSP accompanied by distal amyotrophy have been mapped, for which 13 genes have been identified. With the identification of causative genes, the molecular mechanism of this disease is gradually elucidated.
Databáze: OpenAIRE