Idiopathic AA amyloidosis manifested by autonomic neuropathy, vestibulocochleopathy, and lattice corneal dystrophy.

A 69-year-old Japanese woman with non-familial amyloidosis had polyneuropathy and profound autonomic neuropathy, and kappa chain monoclonal gammopathy. Immunohistopathological examination showed protein AA and protein AP in the amyloid deposits. She showed involvement of the vestibulocochlear nerve...

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Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Tsunoda, I, Awano, H, Kayama, H, Tsukamoto, T, Ueno, S, Fujiwara, T, Watanabe, M, Yamamoto, T
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1994
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1072934/
https://ncbi.nlm.nih.gov/pubmed/8201343
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