Literature DB >> 1568052

Hereditary angioedema complicated with chronic renal failure: report of sibling cases.

H Nomura1, Y Tsugawa, I Koni, Y Tofuku, H Mabuchi, R Takeda, T Sato.   

Abstract

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.

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Year:  1992        PMID: 1568052     DOI: 10.2169/internalmedicine.31.94

Source DB:  PubMed          Journal:  Intern Med        ISSN: 0918-2918            Impact factor:   1.271


  3 in total

Review 1.  Angioedema. Pathogenesis, differential diagnosis, and treatment.

Authors:  Evangelo Frigas; Ugochukwu C Nzeako
Journal:  Clin Rev Allergy Immunol       Date:  2002-10       Impact factor: 8.667

2.  Membranous nephropathy in a patient with hereditary angioedema: a case report.

Authors:  Sandawana W Majoni; Steven R Smith
Journal:  J Med Case Rep       Date:  2008-10-13

Review 3.  The Gut-Kidney Axis: Putative Interconnections Between Gastrointestinal and Renal Disorders.

Authors:  Markku Lehto; Per-Henrik Groop
Journal:  Front Endocrinol (Lausanne)       Date:  2018-09-19       Impact factor: 5.555

  3 in total

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