ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2016
X-linked hypophosphatemic rickets and sagittal craniosynostosis: three patients requiring operative cranial expansion: case series and literature review.
Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.
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Who cites it
14 citing papers in PubMed, 35 citations in OpenAlex.
- X-Linked Hypophosphataemia and Burosumab: A Systemic Disease With a New Treatment.Journal of paediatrics and child health · 2025Review
- Significance of assessing the severity of craniosynostosis in patients with X-linked hypophosphatemia (XLH) at diagnosis.Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology · 2025Article
- X-linked hypophosphatemia due to a de novo novel splice-site variant in a 7-year-old girl with scaphocephaly, Chiari syndrome type I and syringomyelia.Bone reports · 2024Article
- X-linked hypophosphatemia, fibroblast growth factor 23 signaling, and craniosynostosis.Experimental biology and medicine (Maywood, N.J.) · 2023Review
- Review
- Complications in craniosynostosis surgery in patients with rickets: illustrative case and systematic review of literature.Journal of neurosurgery. Case lessons · 2022Article
- Sickle Cell Disease Association with Premature Suture Fusion in Young Children.Plastic and reconstructive surgery. Global open · 2022Article
- Normocephalic sagittal craniosynostosis in young children is common and unrecognized.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2022Article
- X-Linked Hypophosphatemic Rickets: Multisystemic Disorder in Children Requiring Multidisciplinary Management.Frontiers in endocrinology · 2021Review
- Mineralized tissues in hypophosphatemic rickets.Pediatric nephrology (Berlin, Germany) · 2020Review
- Syndromic and Systemic Diagnoses Associated With Isolated Sagittal Synostosis.Plastic and reconstructive surgery. Global open · 2019Article
- The first Korean case report with scaphocephaly as the initial sign of X-linked hypophosphatemic rickets.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2019Article
- High Incidence of Cranial Synostosis and Chiari I Malformation in Children With X-Linked Hypophosphatemic Rickets (XLHR).Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2019Article
- Clinical genetics of craniosynostosis.Current opinion in pediatrics · 2017Review
Corrections and comments
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Authors and funding
4 authors at 3 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
purposeA defect in a phosphate-regulating gene leads to the most common form of rickets: X-linked hypophosphatemic rickets (XLH) or vitamin D-resistant rickets (VDDR). XLH has been associated with craniosynostosis, the sagittal suture being the most commonly involved.
methodsWe present three patients with rickets and symptomatic sagittal suture craniosynostosis all of whom presented late (>2 years of age). Two had a severe phenotype and papilledema, while the third presented with an osseous bulging near the anterior fontanel and experienced chronic headaches.
resultsAll underwent successful cranial vault expansion.
conclusionsRachitic patients with scaphocephaly should be screened for craniosynostosis.
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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.