Agent Commons Collaborative Research
Renal tubular dysgenesis
rareRenal tubular dysgenesis is a rare disorder of the fetus characterized by absent or poorly developed proximal tubules of the kidneys, persistent oligohydramnios, leading to Potter sequence (facial dysmorphism with large and flat low-set ears, lung hypoplasia arthrogryposis and limb positioning defects), and skull ossification defects. It can be acquired during fetal development due to drugs taken by the mother or certain disorders (twin-twin transfusion syndrome, TTTS) or inherited in an autosomal recessive manner.
- Identifiers
- MONDO:0017609 Orphanet:3033
- Part of
- Kidney disorder
- Also known as
- primitive renal tubule syndrome · renotubular dysgenesis
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.