Increased recognition of IgA nephropathy in African-American children.
Based upon the percentage of cases of IgA nephropathy (IgAN) in biopsy series, a lower prevalence has been assumed for African-Americans compared with Americans of European descent.
This may be due to a racial difference in the basic underlying pathology of IgAN or to racial differences in patterns of referral and biopsy selection practices.
Over the past decade (1985-1994), we have found similar incidences of IgAN in Caucasian and African-American children from Shelby County, Tennessee.
The incidence was 3.0 cases per million per year for Caucasian and 5.7 cases per million per year for African-American children.
IgAN may be more common in African-American children than previously appreciated.
Population-based incidence studies will be necessary to determine whether or not our experience has become a more widespread phenomenon.
Mots-clés Pascal : Néphropathie glomérulaire, IgA, Diagnostic, Biopsie, Incidence, Relation, Origine ethnique, Négroïde, Etude statistique, Enfant, Homme, Appareil urinaire pathologie, Rein pathologie, Immunopathologie, Anatomopathologie, Afro-américain
Mots-clés Pascal anglais : Glomerulonephritis, IgA, Diagnosis, Biopsy, Incidence, Relation, Ethnic origin, Negroid, Statistical study, Child, Human, Urinary system disease, Kidney disease, Immunopathology, Pathology, African-amerian
Notice produite par :
Inist-CNRS - Institut de l'Information Scientifique et Technique
Cote : 97-0428370
Code Inist : 002B14A01. Création : 19/12/1997.