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Digitale Medien

Inherited factor H deficiency and collagen type III glomerulopathy (1995)

Vogt, Beth A. ; Wyatt, Robert J. ; Burke, Barbara A. ; [weitere]

Springer

Pediatric nephrology 9 (1995), S. 11-15

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Details

ISSN: 1432-198X

Schlagwort(e): Glomerulonephritis ; Factor H ; Complement ; β-1 H globulin ; Collagen type III glomerulopathy

Quelle: Springer Online Journal Archives 1860-2000

Thema: Medizin

Notizen: Abstract A non-immune complex-mediated glomerulonephritis associated with persistent hypocomplementemia occurred in a young boy. Measurement of complement components revealed complete factor H deficiency, inherited as an autosomal recessive trait. Evaluation of the renal lesion revealed extensive deposition of type III collagen suggestive of collagen type III glomerulopathy, a recently identified cause of chronic renal insufficiency in children and adults. This report represents the first association of inherited factor H deficiency with collagen type III glomerulopathy.

Materialart: Digitale Medien

URL: http://dx.doi.org/10.1007/BF00858956

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