Life paths of patients with transthyretin-related familial amyloid polyneuropathy Val30Met: a descriptive study

Transthyretin-related familial amyloid polyneuropathy Val30Met is a fatal progressive disease. It is a rare hereditary amyloidosis, manifesting as a sensorimotor neuropathy and autonomic dysfunction. It begins during adulthood and is a disabling disease, posing a great psychological burden to patien...

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Bibliographic Details
Main Author: Lopes, A (author)
Other Authors: Sousa, A (author), Fonseca, I (author), Branco, M (author), Rodrigues, C (author), Coelho, T (author), Sequeiros, J (author), Freitas, P (author)
Format: article
Language:eng
Published: 2018
Subjects:
Transthyretin
Familial amyloid polyneuropathy
Amyloidosis
Online Access:http://hdl.handle.net/10216/113023
Country:Portugal
Oai:oai:repositorio-aberto.up.pt:10216/113023

Internet

http://hdl.handle.net/10216/113023

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