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Fig. 3 | BMC Neurology

Fig. 3

From: A novel TTR mutation (p.Ala65Val) underlying late-onset hereditary transthyretin (ATTRv) amyloidosis with mixed cardiac and neuropathic phenotype: a case report

Fig. 3

The patient’s pedigree. The reported patient and his only living brother both show cardiomyopathy (hatched) and polyneuropathy (black shading), and the p.Ala65Val variant. One of the three other brothers suffered cardiomyopathy and polyneuropathy. The patient’s father and two of his brothers died from cardiac events. *own documented evaluation, E (Evaluation) = molecular genetic analysis of the TTR gene

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