Arq. Bras. Cardiol. 2021; 117(5): 1056-1059
Left Ventricular Hypertrophy: One Phenotype, Two Hypotheses, Three Lessons
Patrícia Rodrigues
, Ana Rita Soares, Ricardo Taipa, Sofia Ferreira, Hipólito Reis
Past medical history
A 58-year-old woman with familial amyloid polyneuropathy caused by the Val30Met (p.Val50Met) mutation in the transthyretin (TTR) gene started showing neuropathic symptoms by the age of 37 and a salivary gland biopsy confirmed TTR amyloid deposition. She was submitted to liver transplantation 7 years after symptom onset and was under immunosuppressive drugs, with stable neurological changes since then. She also had chronic kidney failure (stage 3b) and a pacemaker implanted due to sick sinus syndrome.
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Left Ventricular Hypertrophy: One Phenotype, Two Hypotheses, Three Lessons
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