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Cutaneous lymphatic amyloid deposits in ‘Hungarian-type’ familial transthyretin amyloidosis: a case report

✍ Scribed by T. Harkany; F. Garzuly; G. Csanaky; P.G.M. Luiten; C. Nyakas; R.P. Linke; S. Virágh

Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
281 KB
Volume
146
Category
Article
ISSN
0007-0963

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Transthyretin amyloid polyneuropathy, caused by mutations in the transthyretin gene, is a progressive condition for which liver transplantation is an established treatment. Favorable outcomes have been described in patients with the most common transthyretin mutation, Val30Met, but outcomes have bee