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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Autors principals: Tsunoda, I, Awano, H, Kayama, H, Tsukamoto, T, Ueno, S, Fujiwara, T, Watanabe, M, Yamamoto, T
Format: Artigo
Idioma:Inglês
Publicat: 1994
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1072934/
https://ncbi.nlm.nih.gov/pubmed/8201343
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