Foramen magnum stenosis, cervicomedullary decompression, and growth in children with achondroplasia: a retrospective cohort study.

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Title: Foramen magnum stenosis, cervicomedullary decompression, and growth in children with achondroplasia: a retrospective cohort study.
Authors: Fava D; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; Pediatric Endocrinology Unit, Department of Pediatrics, IRCCS Istituto Giannina Gaslini, University of Genoa, Via Gerolamo Gaslini 5, 16147, Genoa, Italy., Angelelli A; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; Pediatric Endocrinology Unit, Department of Pediatrics, IRCCS Istituto Giannina Gaslini, University of Genoa, Via Gerolamo Gaslini 5, 16147, Genoa, Italy., Tedesco C; Pediatric Endocrinology Unit, Department of Pediatrics, IRCCS Istituto Giannina Gaslini, University of Genoa, Via Gerolamo Gaslini 5, 16147, Genoa, Italy., Panciroli M; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy., Bianchin S; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy., Teruzzi D; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy., Scaravilli A; Department of Advanced Biomedical Sciences, University of Naples 'Federico II', Naples, Italy., Pisati A; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy., Barranca I; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy., Scilipoti M; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy., Severino M; Neuroradiology Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy., Napoli F; Pediatric Endocrinology Unit, Department of Pediatrics, IRCCS Istituto Giannina Gaslini, University of Genoa, Via Gerolamo Gaslini 5, 16147, Genoa, Italy., Maiorano NG; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy., Naim A; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy., Negri S; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy., Patti G; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; Pediatric Endocrinology Unit, Department of Pediatrics, IRCCS Istituto Giannina Gaslini, University of Genoa, Via Gerolamo Gaslini 5, 16147, Genoa, Italy., Pistorio A; Scientific Directorate, Epidemiology and Biostatistics Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy., Di Iorgi N; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; Pediatric Endocrinology Unit, Department of Pediatrics, IRCCS Istituto Giannina Gaslini, University of Genoa, Via Gerolamo Gaslini 5, 16147, Genoa, Italy., Allegri AEM; Pediatric Endocrinology Unit, Department of Pediatrics, IRCCS Istituto Giannina Gaslini, University of Genoa, Via Gerolamo Gaslini 5, 16147, Genoa, Italy., Maghnie M; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy. Mohamad.Maghnie@unige.it.; Pediatric Endocrinology Unit, Department of Pediatrics, IRCCS Istituto Giannina Gaslini, University of Genoa, Via Gerolamo Gaslini 5, 16147, Genoa, Italy. Mohamad.Maghnie@unige.it.
Corporate Authors: Skeletal Dysplasia Multidisciplinary Team (GM-MOC)
Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2026 Jan 29; Vol. 21 (1). Date of Electronic Publication: 2026 Jan 29.
Publication Type: Journal Article
Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1750-1172
DOI:10.1186/s13023-026-04219-3