ArticleJournal of Indian Association of Pediatric Surgeons2014
An extremely rare case of classic complete caudal duplication: Dipygus.
Article in Journal of Indian Association of Pediatric Surgeons, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
6 citing papers in PubMed, 9 citations in OpenAlex.
- Disorders of Secondary Neurulation: Suggestion of a New Classification According to Pathoembryogenesis.Advances and technical standards in neurosurgery · 2022Article
- Caudal duplication syndrome: a literature review and reappraisal of its pathoembryogenesis.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021Review
- Disorders of Secondary Neurulation : Mainly Focused on Pathoembryogenesis.Journal of Korean Neurosurgical Society · 2021Article
- Newborn with complete double penis and two separate scrotums: A case report.International journal of surgery case reports · 2020Article
- A case ofVeterinary research forum : an international quarterly journal · 2016Article
- Successful surgical separation of asymmetrical caudal duplication or parasitic twinning in a kitten.JFMS open reportsArticle
Corrections and comments
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Authors and funding
6 authors at 2 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Dipygus is a complete caudal duplication deformity in its severest form. The structures derived from the embryonic cloaca and notochords are duplicated to various extent. We report a male baby who presented to us with complete somatic and visceral duplication below the umbilical level associated with gastroschisis and imperforated anus. Staged surgical corrections were suggested and three out of the four stages were performed successfully.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.