Hereditary gelsolin amyloidosis mimicking Sjögren’s syndrome

Author:

Juusela Pirjo,Tanskanen Maarit,Nieminen Anja,Uitto Veli-Jukka,Blåfield Harri,Kiuru-Enari Sari

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Rheumatology

Reference17 articles.

1. Meretoja J (1969) Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms A previously unrecognized heritable syndrome. Ann Clin Res 4:314–324

2. Kiuru S (1998) Gelsolin-related familial amyloidosis, Finnish type (FAF), and its variants found worldwide. Amyloid 1:55–66

3. Ardalan MR, Shoja MM, Kiuru-Enari S (2007) Amyloidosis-related nephrotic syndrome due to a G654A gelsolin mutation: the first report from the Middle East. Nephrol Dial Transplant 1:272–275. doi: 10.1093/ndt/gfl548 gfl548 [pii]

4. Levy E, Haltia M, Fernandez-Madrid I, Koivunen O, Ghiso J, Prelli F, Frangione B (1990) Mutation in gelsolin gene in Finnish hereditary amyloidosis. J Exp Med 6:1865–1867

5. Page LJ, Suk JY, Huff ME, Lim HJ, Venable J, Yates J, Kelly JW, Balch WE (2005) Metalloendoprotease cleavage triggers gelsolin amyloidogenesis. EMBO J 23:4124–4132

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