Congenital renal anomalies comprise of vast spectrum of pathologies and include:
- renal agenesis
- renal dysgenesis
- congenital megacalyectasis
-
congenital cystic renal disease
- infantile polycystic renal disease: autosomal recessive polycystic kidney disease (ARPKD): Potter type I
- multicystic dysplastic kidneys: Potter type II
- early onset autosomal dominant polycystic kidney disease (ADPKD): Potter type III
- obstructive cystic renal dysplasia: Potter type IV
- obstructive renal disease
- congenital PUJ obstruction
- pretumorous conditions
- renal morphological anomalies
- congenital renal positional anomalies
- tumors presenting in antenatal: childhood period
Associated syndromes
- Bardet-Biedl syndrome
- Beckwith Wiedemann syndrome
- CHARGE syndrome
- fetal alcohol syndrome
- Meckel Gruber syndrome: dominant feature
- Miller Dieker syndrome
- MURCS association: dominant feature
- Noonan syndrome
- Roberts syndrome
- trisomy 13
- VACTERL association: dominant feature