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Hereditary renal amyloidosis caused by a heterozygous G654A gelsolin mutation: a report of two cases
Finnish-type familial amyloidosis (FAF) is a rare hereditary systemic amyloidosis that mainly exhibits cranial neuropathy. We describe a Japanese family with FAF manifested predominantly as renal amyloidosis. The proband was a 42-year-old woman with a 21-year history of proteinuria due to renal amyl...
Zapisane w:
| Wydane w: | Clin Kidney J |
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| Główni autorzy: | , , , , , |
| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
Oxford University Press
2013
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| Hasła przedmiotowe: | |
| Dostęp online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4432447/ https://ncbi.nlm.nih.gov/pubmed/26019848 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ckj/sft007 |
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