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• W4200028615 endingPage "36" @default.
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• W4200028615 abstract "Transthyretin amyloidosis (ATTR-amyloidosis) is a systemic progressive fatal disease, for which a modifying therapy has recently been proposed that delays the progression of the disease and improves the patient’s quality of life. The delay in the diagnosis of ATTR-amyloidosis is associated with the heterogeneity of the manifestations of the disease, as well as insufficient awareness of doctors of different specialties about the disease. A review of recent studies on the symptomatology, diagnosis, molecular genetic characteristics of ATTR-amyloidosis and the most common forms of the disease with the predominant involvement of peripheral nerves and the heart, as well as the kidneys, gastrointestinal tract, and eyes is presented. The international consensus recommendations for the diagnosis of suspected ATTR-amyloidosis using modern methods that facilitate early and accurate diagnosis are discussed. The reasons and the most frequent misdiagnoses of ATTR-amyloidosis, which also lead to a delay in the timely appointment of therapy, are considered. Molecular genetic testing should be considered early in the evaluation of a patient with unexplained peripheral neuropathy and cardiomyopathy. A diagnostic algorithm based on the initial symptoms and manifestations of the cardiovascular and nervous systems facilitates the identification of a patient with clinical suspicion of ATTR-amyloidosis by the general practitioner. Early diagnosis is critically important for patients with ATTR polyneuropathy, since the early prescription of Vindakel (tafamidis), registered in the Russian Federation in 2017, allows a significant clinical effect to be obtained. Timely administration of Vindakel significantly slows down the progression of the disease, improves the prognosis and quali ty of life in patients with ATTR polyneuropathy." @default.
• W4200028615 created "2021-12-31" @default.
• W4200028615 creator A5015696627 @default.
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• W4200028615 creator A5087180875 @default.
• W4200028615 date "2021-12-13" @default.
• W4200028615 modified "2023-09-30" @default.
• W4200028615 title "Phenotypic heterogeneity and diagnostic features of transthyretin amyloidosis with polyneuropathy" @default.
• W4200028615 cites W1120283132 @default.
• W4200028615 cites W1504652596 @default.
• W4200028615 cites W1553593663 @default.
• W4200028615 cites W1558011912 @default.
• W4200028615 cites W1793435044 @default.
• W4200028615 cites W1883283575 @default.
• W4200028615 cites W189397201 @default.
• W4200028615 cites W1899949139 @default.
• W4200028615 cites W1903745637 @default.
• W4200028615 cites W1970113480 @default.
• W4200028615 cites W1970793380 @default.
• W4200028615 cites W1973342497 @default.
• W4200028615 cites W1975536578 @default.
• W4200028615 cites W1977354928 @default.
• W4200028615 cites W1977614036 @default.
• W4200028615 cites W1979219069 @default.
• W4200028615 cites W1980144587 @default.
• W4200028615 cites W1981089609 @default.
• W4200028615 cites W1982873078 @default.
• W4200028615 cites W1984035915 @default.
• W4200028615 cites W1986782676 @default.
• W4200028615 cites W1993848195 @default.
• W4200028615 cites W1994321237 @default.
• W4200028615 cites W1995391002 @default.
• W4200028615 cites W1996927016 @default.
• W4200028615 cites W2001044311 @default.
• W4200028615 cites W2005678387 @default.
• W4200028615 cites W2005769831 @default.
• W4200028615 cites W2008138501 @default.
• W4200028615 cites W2012206867 @default.
• W4200028615 cites W2013486441 @default.
• W4200028615 cites W2013703514 @default.
• W4200028615 cites W2018190103 @default.
• W4200028615 cites W2019261756 @default.
• W4200028615 cites W2020348130 @default.
• W4200028615 cites W2021400053 @default.
• W4200028615 cites W2024354301 @default.
• W4200028615 cites W2026704636 @default.
• W4200028615 cites W2030399712 @default.
• W4200028615 cites W2038521258 @default.
• W4200028615 cites W2042267589 @default.
• W4200028615 cites W2047948719 @default.
• W4200028615 cites W2059460247 @default.
• W4200028615 cites W2060592636 @default.
• W4200028615 cites W2060624358 @default.
• W4200028615 cites W2061527271 @default.
• W4200028615 cites W2065886751 @default.
• W4200028615 cites W2067050589 @default.
• W4200028615 cites W2072802176 @default.
• W4200028615 cites W2074628855 @default.
• W4200028615 cites W2075960572 @default.
• W4200028615 cites W2076492105 @default.
• W4200028615 cites W2080914865 @default.
• W4200028615 cites W2089396544 @default.
• W4200028615 cites W2091551497 @default.
• W4200028615 cites W2096319356 @default.
• W4200028615 cites W2097298883 @default.
• W4200028615 cites W2101934278 @default.
• W4200028615 cites W2102574907 @default.
• W4200028615 cites W2106217022 @default.
• W4200028615 cites W2114075554 @default.
• W4200028615 cites W2115716349 @default.
• W4200028615 cites W2115862827 @default.
• W4200028615 cites W2116135450 @default.
• W4200028615 cites W2117942418 @default.
• W4200028615 cites W2122861669 @default.
• W4200028615 cites W2123950122 @default.
• W4200028615 cites W2126501528 @default.
• W4200028615 cites W2128307213 @default.
• W4200028615 cites W2128789805 @default.
• W4200028615 cites W2130506624 @default.
• W4200028615 cites W2131999691 @default.
• W4200028615 cites W2133199265 @default.
• W4200028615 cites W2133745249 @default.
• W4200028615 cites W2137399373 @default.
• W4200028615 cites W2143446051 @default.
• W4200028615 cites W2144376654 @default.
• W4200028615 cites W2154120519 @default.
• W4200028615 cites W2155971024 @default.
• W4200028615 cites W2158021885 @default.
• W4200028615 cites W2158280929 @default.
• W4200028615 cites W2159558124 @default.
• W4200028615 cites W2160966221 @default.
• W4200028615 cites W2162772358 @default.
• W4200028615 cites W2163584170 @default.
• W4200028615 cites W2164614237 @default.

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