Apolipoprotein A-1-related amyloidosis 2 case reports and review of the literature

RATIONALE: Apolipoprotein A-1 (ApoA-1)-related amyloidosis is characterized by the deposition of ApoA-1 in various organs and can be either hereditary or nonhereditary. It is rare and easily misdiagnosed. Renal involvement is common in hereditary ApoA-1 amyloidosis, but rare in the nonhereditary for...

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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Medicine (Baltimore)
Asıl Yazarlar: Lu, Chunlei, Zuo, Ke, Lu, Yinghui, Liang, Shaoshan, Huang, Xianghua, Zeng, Caihong, Zhang, Jiong, An, Yu, Wang, Jinquan
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Wolters Kluwer Health 2017
Konular:
5200
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5626298/
https://ncbi.nlm.nih.gov/pubmed/28953655
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000008148
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