Hereditary angioedema complicated with chronic renal failure: report of sibling cases.
スポンサーリンク
概要
- 論文の詳細を見る
Hereditary angioedema (HAE) is known as a deficiency state of C1 inhibitor (C1 INH), an important protease inhibitor protein involved in the complement system. As with other components of the classical pathway of the complement system, a state of its deficiency often causes clinical immunoregulatory disorders. A 45-yr-old brother and a 63-yr-old sister with HAE both developed chronic renal failure, probably due to chronic glomerulonephritis, and required regular hemodialysis. This is, to our knowledge, the first report of sibling cases of HAE associated with chronic renal failure.
- 日本内科学会の論文
著者
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MABUCHI Hiroshi
The Second Department of Internal Medicine, School of Medicine, Kanazawa University
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Takeda Ryoyu
The Second Department of Internal Medicine, School of Medicine, Kanazawa University
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SATO Takashi
the Department of Urology,Oji General Hospital
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Takeda Ryoyu
The Second Department Of Internal Medicine Kanazawa University School Of Medicine.
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Mabuchi Hiroshi
The Second Department Of Internal Medicine
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Koni Ichiro
The Second Department Of Internal Medicine Kanazawa University School Of Medicine
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TOFUKU Yohei
The Second Department of Internal Medicine, School of Medicine, Kanazawa University
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Nomura Hideki
The Second Department of Internal Medicine, School of Medicine, Kanazawa University
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Tsugawa Yoshinori
The Second Department of Internal Medicine, School of Medicine, Kanazawa University
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KONI Ichiro
The Second Department of Internal Medicine, School of Medicine, Kanazawa University
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