We describe a child with isolated haematuria who was diagnosed and successf
ully treated for idiopathic hypercalciuria for 6 months, after which IgA ne
phropathy was demonstrated on renal biopsy performed due to the relapse of
haematuria in spite of low calciuria levels. To our knowledge, this is the
first case evaluated systematically in the literature shown to have IgA nep
hropathy while being followed up for idiopathic hypercalciuria.