Demographic and clinical characteristics of children with autosomal dominant polycystic kidney disease: a single center experience
Belde Kasap-DemirFatma MutlubaşEren SoyaltınCaner AlparslanMerve AryaDemet AlaygutSeçil Arslansoyu ÇamlarAfig BerdeliOnder YavascanPublished in: Turkish journal of medical sciences (2021)
The majority of children with ADPKD had preserved renal functions and slight cyst enlargement during their follow-up. However, they may have different renal problems deserving closed follow-up.