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Updated: Jan 15, 2026

Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis
Published on: June 9, 2018
Long-Term Peritoneal Dialysis in Hereditary Transthyretin Amyloidosis: A Case Report and Management Challenges
Vítor Fernandes1, Núria Paulo1, Roberto Silva2
1Nephrology, Unidade Local de Saúde de São João, Porto, PRT.
Abstract:
Amyloidosis is a disease characterized by extracellular deposition of misfolded proteins, causing progressive organ damage, including end-stage kidney disease (ESKD). Patients with ESKD due to amyloidosis face poor survival rates, and evidence to guide optimal management strategies is lacking. We present the case of a 64-year-old woman with hereditary transthyretin (TTR) amyloidosis and ESKD who has been successfully treated with peritoneal dialysis (PD) for over 33 months. This report highlights the challenges encountered during follow-up, including the progression of peripheral neuropathy, and underscores the need for further investigation leading to targeted therapies to prevent disease progression and complications.
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