A case with a novel variant transthyretin A36D presenting cardiac phenotype

Toshiya NomuraDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, JapanCorrespondence[email protected]

Taro YamashitaDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan

Yohei MisumiDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan

Mitsuharu UedaDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan

Teruaki MasudaDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan

Masayoshi TasakiDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan

Yukio AndoDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan

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References

Coelho T, Maia LF, Martins da Silva A, Waddington Cruz M, Planté-Bordeneuve V, Lozeron P, Suhr OB, et al. Tafamidis for transthyretin familial amyloid polyneuropathy: a randomized, controlled trial. Neurology 2012;79:785–92.
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Ericzon BG, Wilczek HE, Larsson M, Wijayatunga P, Stangou A, Pena JR, Furtado E, et al. Liver transplantation for hereditary transthyretin amyloidosis: after 20 years still the best therapeutic alternative? Transplantation 2015;99:1847–54.
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Kon T, Misumi Y, Nishijima H, Honda M, Suzuki C, Baba M, Inomata Y, et al. Effects of liver transplantation and tafamidis in hereditary transthyretin amyloidosis caused by transthyretin Leu55Pro mutation: a case report. Amyloid 2015;22:203–4.
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A case with a novel variant transthyretin A36D presenting cardiac phenotype

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A case with a novel variant transthyretin A36D presenting cardiac phenotype

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