bilateral multicystic kidneys
bilateral diffuse multicystic kidneys
Etiology
polycystic kidney diseases (PKDs)
- autosomal recessive polycystic kidney diseases (ARPKD)
- autosomal dominant polycystic kidney diseases (ADPKD)
bilateral multicystic renal dysplasia (BMRD)
- obstructive bilateral multicystic renal dysplasia (OBMRD)
- non-obstructive bilateral multicystic renal dysplasia (NOBMRD)
- isolated NOBMRD
- syndromal NOBMRD
- Meckel disease (exemple)
Bilateral diffuse multicystic kidneys - 22 weeks male fetus. No other malformation associated. Ureteres are not dilated. Etiology unknown.
Bilateral diffuse multicystic kidneys - 22 weeks male fetus. No other malformation associated. Ureteres are not dilated. Etiology unknown. (After formalin fixation)
Bilateral diffuse multicystic kidneys - 22 weeks male fetus. No other malformation associated. Ureteres are not dilated. Etiology unknown.
Renal ARPKD - 39 weeks.
Bilateral multicystic renal dysplasia (19 weeks) - Severe caudal regression syndrome with vesical agenesis
Bilateral non-obstructive multicystic renal dysplasia (BNOMRD)
Bilateral non-obstructive multicystic renal dysplasia (BNOMRD)
Bilateral non-obstructive multicystic renal dysplasia (BNOMRD) (21 weeks) - Malformative syndrome associating cardiac anomalies (dextrocardia, situs inversus, right aortic arch, pulnoary atresia, ventricular septal defect), cleft lip/palate, unicorn uterus with right tubar agenesis).
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