Autosomal dominant polycystic kidney disease (ADPKD)
ADPKD usually manifests in the middle-aged period of life but many cases are discovered earlier when workup is
done because of family history. In this section one sees interstitial fibrosis and cysts. In some other sections it would
be likely to see a few residual glomeruli. Rarely, this disease presents in a fetus or neonate.