Genetic and clinical features of pediatric-onset hereditary spastic paraplegia: a single-center study in Japan.

Ikeda, Azusa; Kumaki, Tatsuro; Tsuyusaki, Yu; Tsuji, Megumi; Enomoto, Yumi; Fujita, Atsushi; Saitsu, Hirotomo; Matsumoto, Naomichi; Kurosawa, Kenji; Goto, Tomohide

Ikeda, Azusa; Kumaki, Tatsuro; Tsuyusaki, Yu; Tsuji, Megumi; Enomoto, Yumi; Fujita, Atsushi; Saitsu, Hirotomo; Matsumoto, Naomichi; Kurosawa, Kenji; Goto, Tomohide.

Afiliação

Ikeda A; Department of Neurology, Kanagawa Children's Medical Center, Yokohama, Japan.
Kumaki T; Division of Medical Genetics, Kanagawa Children's Medical Center, Yokohama, Japan.
Tsuyusaki Y; Department of Neurology, Kanagawa Children's Medical Center, Yokohama, Japan.
Tsuji M; Department of Neurology, Kanagawa Children's Medical Center, Yokohama, Japan.
Enomoto Y; Clinical Research Institute, Kanagawa Children's Medical Center, Yokohama, Japan.
Fujita A; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Saitsu H; Department of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Matsumoto N; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Kurosawa K; Division of Medical Genetics, Kanagawa Children's Medical Center, Yokohama, Japan.
Goto T; Department of Neurology, Kanagawa Children's Medical Center, Yokohama, Japan.

Front Neurol ; 14: 1085228, 2023.

Article em En | MEDLINE | ID: mdl-37251230

Palavras-chave

diagnostic yield; genetic sequencing; hereditary spastic paraplegia; pediatric-onset hereditary spastic paraplegia; sporadic

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Front Neurol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Japão

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