[Case of hereditary Y69H (p.Y89H) transthyretin variant leptomeningeal amyloidosis presenting with drop attacks and recurrent transient language disorder].

Saito, Natsumi; Kuroha, Yasuko; Hasegawa, Arika; Tada, Mari; Kakita, Akiyoshi; Watanabe, Kei; Takahashi, Tetsuya

Saito, Natsumi; Kuroha, Yasuko; Hasegawa, Arika; Tada, Mari; Kakita, Akiyoshi; Watanabe, Kei; Takahashi, Tetsuya.

Afiliação

Saito N; Department of Neurology, NHO Nishiniigata Chuo Hospital.
Kuroha Y; Department of Neurology, NHO Nishiniigata Chuo Hospital.
Hasegawa A; Department of Neurology, NHO Nishiniigata Chuo Hospital.
Tada M; Department of Pathology, Brain Research Institute, Niigata University.
Kakita A; Department of Pathology, Brain Research Institute, Niigata University.
Watanabe K; Department of Orthopedic Surgery, Niigata University School of Medicine.
Takahashi T; Department of Neurology, NHO Nishiniigata Chuo Hospital.

Rinsho Shinkeigaku ; 63(10): 650-655, 2023 Oct 25.

Article em Ja | MEDLINE | ID: mdl-37779024

Assuntos

Neuropatias Amiloides Familiares; Afasia; Humanos; Feminino; Idoso; Pré-Albumina/genética; Neuropatias Amiloides Familiares/complicações; Neuropatias Amiloides Familiares/diagnóstico; Neuropatias Amiloides Familiares/genética; Síncope

Palavras-chave

Y69H; drop attack; leptomeningeal amyloidosis; logopenic variant of primary progressive aphasia; transthyretin amyloidosis

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Afasia / Neuropatias Amiloides Familiares Limite: Aged / Female / Humans Idioma: Ja Revista: Rinsho Shinkeigaku Ano de publicação: 2023 Tipo de documento: Article

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