congenital renal disease
Congenital
seminal vesicle cyst in Zinner syndrome. CT with coronal reformation showing absence of the right kidney and reduced size of the left kidney
Renal
dysgenesis • Congenital hypoplastic kidney - Ganzer Fall bei Radiopaedia
Renal
agenesis • Unilateral renal agenesis - Ganzer Fall bei Radiopaedia
Horseshoe
kidney • Horseshoe kidney - Ganzer Fall bei Radiopaedia
Congenital
renal anomalies • Multicystic dysplastic kidney - Ganzer Fall bei Radiopaedia
Autosomal
recessive polycystic kidney disease • Autosomal recessive polycystic kidney disease - Ganzer Fall bei Radiopaedia
Congenital
renal anomalies • Pelviureteric junction obstruction (PUJ) - Ganzer Fall bei Radiopaedia
Congenital
renal anomalies • Pelvic kidney - Ganzer Fall bei Radiopaedia
Congenital
renal anomalies • Duplex kidney with triple renal arteries - Ganzer Fall bei Radiopaedia
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
- pre-tumourous conditions
- renal morphological anomalies
- horseshoe kidney
- cross fused renal ectopia
- Fused supernumerary kidneys
- 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
- trisomy 13
- Roberts syndrome
- VACTERL association: dominant feature
See also
Siehe auch:
- junktionaler Parenchymdefekt der Niere
- Pätau-Syndrom
- Hufeisenniere
- Meckel-Syndrom
- Ureterabgangsstenose
- multizystische Nierendysplasie
- VACTERL-Assoziation
- Malrotation der Niere
- Beckwith-Wiedemann-Syndrom
- einseitige Nierenagenesie
- Roberts-Syndrom
- Nephroblastomatose
- autosomal-dominante polyzystische Nierenerkrankung
- Bardet-Biedl syndrome
- CHARGE-Syndrom
- Nephroblastom
- Noonan-Syndrom
- Fetales Alkoholsyndrom
- Nierenhypoplasie
- obstructive cystic renal dysplasia
- gekreuzte Nierendystopie mit Verschmelzung
- developmental anomalies of the kidney
- fused pelvic kidney
- MURCS association
- autosomal recessive polycystic kidney disease (ARPKD)
- multilokuläres zystisches Nephrom
- congenital cystic renal disease
- Nierendysgenesie
- kongenitales mesoblastisches Nephrom
- Miller-Dieker Syndrom
- multicystic dysplastic kidneys
- Megakalikose
und weiter:
Assoziationen und Differentialdiagnosen zu angeborene renale Anomalien:
junktionaler
Parenchymdefekt der Niere
autosomal
recessive polycystic kidney disease (ARPKD)
