Congenital renal anomalies
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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-tumourous conditions - renal morphological anomalies
- congenital renal positional anomalies
- tumours 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
-<li>pre tumourous conditions<ul><li><a href="/articles/nephroblastomatosis">nephroblastomatosis</a></li></ul>- +<li>pre-tumourous conditions<ul><li><a href="/articles/nephroblastomatosis">nephroblastomatosis</a></li></ul>
Images Changes:
Image 1 CT (renal cortical phase) ( update )
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Case 1 -: congenital renal hypoplasia - on right
Image 2 CT (non-contrast) ( update )
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Case 2 -: unilateral right renal agenesis
Image 3 CT (C+ portal venous phase) ( update )
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Case 3 -: horseshoe kidney
Image 4 Ultrasound ( update )
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Case 4 -: multicystic dysplastic kidney
Image 5 MRI (T1 fat sat) ( update )
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Case 5 -: ARPKD
Image 6 CT (non-contrast) ( update )
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Case 6 -: PUJ obstruction
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