PedAM
Pediatric Disease Annotations & Medicines
| Disease | anuria |
| Phenotype | C0079924|oligohydramnios |
| Sentences | 5 |
| PubMedID- 23636579 | Renal tubular dysgenesis (rtd) is a severe foetal disorder characterised by the absence or poor development of proximal tubules, early onset and persistent anuria (leading to oligohydramnios and the potter sequence) and ossification defects of the skull. |
| PubMedID- 26000015 | In human studies, the most commonly reported adverse effects of aceis or arbs taken in the second or third trimester include suppressed fetal renal function and reduced urine output, which lead to oligohydramnios with fetal anuria, neonatal hypotension, renal failure, and hypocalvaria [96–99]. |
| PubMedID- 22203847 | anuria associated with oligohydramnios may produce fetal limb contractures, craniofacial deformities, and pulmonary hypoplasia. |
| PubMedID- 22095942 | Autosomal recessive renal tubular dysgenesis (rtd) is a severe disorder of renal tubular development characterized by early onset and persistent fetal anuria leading to oligohydramnios and the potter sequence, associated with skull ossification defects. |
| PubMedID- 19924102 | Autosomal recessive renal tubular dysgenesis (rtd) is a severe disorder of renal tubular development characterized by early onset and persistent fetal anuria leading to oligohydramnios and the potter sequence. |
Page: 1