Clinical and genetic characterization of a Taiwanese cohort with spastic paraparesis combined with cerebellar involvement.

Lan, Min-Yu; Lu, Chin-Song; Wu, Shey-Lin; Chen, Ying-Fa; Sung, Yueh-Feng; Tu, Min-Chien; Chang, Yung-Yee

Lan, Min-Yu; Lu, Chin-Song; Wu, Shey-Lin; Chen, Ying-Fa; Sung, Yueh-Feng; Tu, Min-Chien; Chang, Yung-Yee.

Afiliação

Lan MY; Department of Neurology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
Lu CS; Center for Parkinson's Disease, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
Wu SL; Center for Mitochondrial Research and Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
Chen YF; Professor Lu Neurological Clinic, Taoyuan, Taiwan.
Sung YF; Department of Neurology, Landseed International Hospital, Taoyuan, Taiwan.
Tu MC; Department of Neurology, Changhua Christian Hospital, Changhua, Taiwan.
Chang YY; Department of Electrical Engineering, National Changhua University of Education, Changhua, Taiwan.

Front Neurol ; 13: 1005670, 2022.

Article em En | MEDLINE | ID: mdl-36247768

Palavras-chave

ataxia-spasticity spectrum diseases; hereditary spastic paraplegia; spinocerebellar ataxia; thin corpus callosum; whole-exome sequencing

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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Front Neurol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Taiwan

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