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An acquired form of renal tubular dysgenesis that develops in donor fetuses due to the uneven shunting of growth factor and nutrients to the kidney of the recipient and is characterized by absent or poorly developed proximal tubules, persistent oligohydramnios and consequently the Potter sequence (facial dysmorphism with large and flat low-set ears, lung hypoplasia, arthrogryposis and limb positioning defects).
Biomarker and diagnostic research for renal tubular dysgenesis due to twin-twin transfusion has been reported in the published literature.
No clinical trials have been registered for renal tubular dysgenesis due to twin-twin transfusion.
4 publications have been identified in PubMed for renal tubular dysgenesis due to twin-twin transfusion. Research spans Case Report / Case Series (50%), Diagnostic / Biomarker (25%), and Review / Meta-Analysis (25%).
Sugita R (2026). [PMID: 41212229](https://pubmed.ncbi.nlm.nih.gov/41212229/). *Pediatr Nephrol*. [Case Report / Case Series]
Varughese R (2025). [PMID: 39891580](https://pubmed.ncbi.nlm.nih.gov/39891580/). *Endocr Rev*. [Review / Meta-Analysis]
Paiva Ferreira I (2025). [PMID: 39991384](https://pubmed.ncbi.nlm.nih.gov/39991384/). *Cureus*. [Case Report / Case Series]
Hasan Z (2025). [PMID: 40080703](https://pubmed.ncbi.nlm.nih.gov/40080703/). *Br J Radiol*. [Diagnostic / Biomarker]
Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 10:20 PM UTC
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