ArticleJournal of pediatric neurosciences2014
Rare association of spondylo costal dysostosis with split cord malformations type II: A case report and a brief review of literature.
Article in Journal of pediatric neurosciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 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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Who cites it
4 citing papers in PubMed, 5 citations in OpenAlex.
- Prevalence and Recurrence of Lower-Limb Deformities in Jarcho-Levin Syndrome: A Single-Center Retrospective Cohort Study.Children (Basel, Switzerland) · 2026Article
- Integration of molecular diagnostics and karyotyping for enhanced detection of chromosomal abnormalities in fetuses.Archives of medical science : AMS · 2025Article
- Spondylocostal dysostosis with type II split cord malformation: A report of a rare case and brief review of the literature.Radiology case reports · 2024Article
- Jarcho-Levin syndrome with diastematomyelia and a dorsal dermal sinus.Radiology case reports · 2024Article
Corrections and comments
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Spondylo costal dysostosis (SCD) is a genetic skeletal disorder characterized by a variety of costo-vertebral malformations. SCD with type I split cord malformation (SCM) have been reported in the literature. We report an unusual association of SCD with type II SCM. Imaging studies revealed multiple vertebral segmentations, rib malformations, spina bifida and low lying cord with type II SCM at the D12-L3 level. She underwent detethering of the cord. To the best of our knowledge, this is the first report of the association of SCD with type II SCM.
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Registered trials
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