Rare genetic variant in the CFB gene presenting as atypical hemolytic uremic syndrome and immune complex diffuse membranoproliferative glomerulonephritis, with crescents, successfully treated with eculizumab. [electronic resource]
Producer: 20180307Description: 885-891 p. digitalISSN:- 1432-198X
- Antibodies, Monoclonal, Humanized -- therapeutic use
- Child
- Complement C3 -- analysis
- Complement Factor B -- genetics
- Creatinine -- blood
- DNA Mutational Analysis
- Exons -- genetics
- Glomerulonephritis, Membranoproliferative -- drug therapy
- Hemolytic-Uremic Syndrome -- drug therapy
- Humans
- Kidney Failure, Chronic -- prevention & control
- Kidney Function Tests
- Male
- Mutation
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Publication Type: Journal Article
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