| Literature DB >> 34731448 |
José Berciano1, José Gazulla2, Jon Infante3.
Abstract
The aim of this paper is to carry out a historical overview of the evolution of the knowledge on degenerative cerebellar disorders and hereditary spastic paraplegias, over the last century and a half. Original descriptions of the main pathological subtypes, including Friedreich's ataxia, hereditary spastic paraplegia, olivopontocerebellar atrophy and cortical cerebellar atrophy, are revised. Special attention is given to the first accurate description of striatonigral degeneration by Hans Joachim Scherer, his personal and scientific trajectory being clarified. Pathological classifications of ataxia are critically analysed. The current clinical-genetic classification of ataxia is updated by taking into account recent molecular discoveries. We conclude that there has been an enormous progress in the knowledge of the nosology of hereditary ataxias and paraplegias, currently encompassing around 200 genetic subtypes.Entities:
Keywords: Ataxia; Autosomal dominant cerebellar ataxia; Autosomal recessive cerebellar ataxia; Cortical cerebellar atrophy; Episodic ataxia; Friedreich’s ataxia; Hans Joachim Scherer; Hereditary spastic paraplegia; Idiopathic late-onset ataxia; Multiple system atrophy; Nazism; Non-progressive congenital ataxia; Olivopontocerebellar atrophy; Parkinsonism; SCA genes; SPG genes; Sporadic adult-onset ataxia; Striatonigral degeneration
Mesh:
Year: 2021 PMID: 34731448 DOI: 10.1007/s12311-021-01328-6
Source DB: PubMed Journal: Cerebellum ISSN: 1473-4222 Impact factor: 3.648