Accelerating restrictive cardiomyopathy after liver transplantation in a patient with familial amyloidotic polyneuropathy: a case report

INTRODUCTION: Hereditary amyloidodis is a rare disease process with a propensity to cause polyneuropathies, autonomic dysfunction, and restrictive cardiomyopathy. It is transmitted in an autosomal dominant manner, with disease onset usually in the 20s-40s. The most common hereditary amyloidogenic pr...

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Detalles Bibliográficos
Autores principales: Robin, Jason, Meyers, Sheridan, Nahlawi, Maher, Puthumana, Jyothy, Lomasney, Jon, Mehlman, David, Rigolin, Vera, Davidson, Charles
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2248590/
https://www.ncbi.nlm.nih.gov/pubmed/18241340
http://dx.doi.org/10.1186/1752-1947-2-35

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2248590/
https://www.ncbi.nlm.nih.gov/pubmed/18241340
http://dx.doi.org/10.1186/1752-1947-2-35

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