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Features include: Rectovaginal fistula and Anal atresia.
Biomarker and diagnostic research for hereditary anorectal anomalies has been reported in the published literature.
No clinical trials have been registered for hereditary anorectal anomalies.
60 publications have been identified in PubMed for hereditary anorectal anomalies. Research spans Case Report / Case Series (38%), Basic Science / Preclinical (17%), and Epidemiology / Natural History (17%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 23 | 38% |
Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 6:26 AM UTC
Online Mendelian Inheritance in Man
Laboratory research
10 |
17% |
Disease patterns and progression | 10 | 17% |
Research summaries | 8 | 13% |
Testing and diagnosis research | 5 | 8% |
New treatment approaches | 2 | 3% |
Other research | 1 | 2% |
Clinical study results | 1 | 2% |
Schwarz RB (2026). [PMID: 41871657](https://pubmed.ncbi.nlm.nih.gov/41871657/). *J Pediatr Surg*. [Epidemiology / Natural History]
Langer S (2026). [PMID: 41513036](https://pubmed.ncbi.nlm.nih.gov/41513036/). *J Pediatr Surg*. [Review / Meta-Analysis]
Jung JH (2026). [PMID: 41486773](https://pubmed.ncbi.nlm.nih.gov/41486773/). *J Yeungnam Med Sci*. [Case Report / Case Series]
Firn K (2026). [PMID: 40465813](https://pubmed.ncbi.nlm.nih.gov/40465813/). *Unknown Journal*. [Other]
Wang X (2026). [PMID: 41871837](https://pubmed.ncbi.nlm.nih.gov/41871837/). *Congenit Anom (Kyoto)*. [Case Report / Case Series]
Ürkmez MF (2026). [PMID: 41499068](https://pubmed.ncbi.nlm.nih.gov/41499068/). *CEN Case Rep*. [Case Report / Case Series]
Suseelan V (2026). [PMID: 42058895](https://pubmed.ncbi.nlm.nih.gov/42058895/). *iScience*. [Epidemiology / Natural History]
Yan L (2026). [PMID: 41923049](https://pubmed.ncbi.nlm.nih.gov/41923049/). *BMC Med Genomics*. [Gene Therapy / Novel Therapeutics]
Wang C (2026). [PMID: 42228139](https://pubmed.ncbi.nlm.nih.gov/42228139/). *Pediatr Surg Int*. [Gene Therapy / Novel Therapeutics]
Feng X (2026). [PMID: 40605465](https://pubmed.ncbi.nlm.nih.gov/40605465/). *Clinical genetics*. [Case Report / Case Series]