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Prevalence of IgA2 Deposits in IgA Nephropathies — A Clue to Their Pathogenesis

List of authors.
  • Claude André, M.D.,
  • François Claude Berthoux, M.D.,
  • Françoise André, B.Sc.,
  • John Gillon, M.R.C.P.,
  • Christian Genin, M.D.,
  • and Jean-Charles Sabatier, M.D.

GLOMERULAR deposits of IgA are common and are thought to play an important part in the pathogenesis of several different diseases. Primary IgA nephropathy (Berger's disease) is a common type of glomerulonephritis that occurs chiefly in early adult life; the patient presents with a history of recurrent episodes of macroscopic or microscopic hematuria. The onset of symptoms has been reported to coincide with or follow soon after an upper-respiratory-tract infection or gastroenteritis. Renal impairment is usually mild, but some patients progress to end-stage renal failure, and the disease tends to recur in grafted kidneys after transplantation.1 Glomerular lesions characterized by . . .

Funding and Disclosures

Supported by an INSERM Grant (ATP 78/79–110 Contrat 001).

We are indebted to Miss M. C. Fargier and Mr. G. Jourdan for expert technical assistance.

Author Affiliations

From Unité 45 INSERM, Hôpital Edouard Herriot, Lyons, and Service de Néphrologie, Hôpital Bellevue, St. Etienne, France. Address reprint requests to Dr. Claude André at Unité de Recherche de physiopathologic Digestive, INSERM U 45, Pav. H, Hôpital E. Herriot, 69374 Lyon Cedex 2, France.

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