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. |
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| 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 |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 41612394 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Foramen magnum stenosis, cervicomedullary decompression, and growth in children with achondroplasia: a retrospective cohort study. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Fava+D%22">Fava D</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Angelelli+A%22">Angelelli A</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Tedesco+C%22">Tedesco C</searchLink>; Pediatric Endocrinology Unit, Department of Pediatrics, IRCCS Istituto Giannina Gaslini, University of Genoa, Via Gerolamo Gaslini 5, 16147, Genoa, Italy.<br /><searchLink fieldCode="AU" term="%22Panciroli+M%22">Panciroli M</searchLink>; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.<br /><searchLink fieldCode="AU" term="%22Bianchin+S%22">Bianchin S</searchLink>; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.<br /><searchLink fieldCode="AU" term="%22Teruzzi+D%22">Teruzzi D</searchLink>; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.<br /><searchLink fieldCode="AU" term="%22Scaravilli+A%22">Scaravilli A</searchLink>; Department of Advanced Biomedical Sciences, University of Naples 'Federico II', Naples, Italy.<br /><searchLink fieldCode="AU" term="%22Pisati+A%22">Pisati A</searchLink>; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.<br /><searchLink fieldCode="AU" term="%22Barranca+I%22">Barranca I</searchLink>; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.<br /><searchLink fieldCode="AU" term="%22Scilipoti+M%22">Scilipoti M</searchLink>; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.<br /><searchLink fieldCode="AU" term="%22Severino+M%22">Severino M</searchLink>; Neuroradiology Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.<br /><searchLink fieldCode="AU" term="%22Napoli+F%22">Napoli F</searchLink>; Pediatric Endocrinology Unit, Department of Pediatrics, IRCCS Istituto Giannina Gaslini, University of Genoa, Via Gerolamo Gaslini 5, 16147, Genoa, Italy.<br /><searchLink fieldCode="AU" term="%22Maiorano+NG%22">Maiorano NG</searchLink>; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.<br /><searchLink fieldCode="AU" term="%22Naim+A%22">Naim A</searchLink>; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.<br /><searchLink fieldCode="AU" term="%22Negri+S%22">Negri S</searchLink>; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.<br /><searchLink fieldCode="AU" term="%22Patti+G%22">Patti G</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Pistorio+A%22">Pistorio A</searchLink>; Scientific Directorate, Epidemiology and Biostatistics Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.<br /><searchLink fieldCode="AU" term="%22Di+Iorgi+N%22">Di Iorgi N</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Allegri+AEM%22">Allegri AEM</searchLink>; Pediatric Endocrinology Unit, Department of Pediatrics, IRCCS Istituto Giannina Gaslini, University of Genoa, Via Gerolamo Gaslini 5, 16147, Genoa, Italy.<br /><searchLink fieldCode="AU" term="%22Maghnie+M%22">Maghnie M</searchLink>; 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. – Name: AuthorCorporate Label: Corporate Authors Group: Au Data: <searchLink fieldCode="CA" term="%22Skeletal+Dysplasia+Multidisciplinary+Team+%28GM-MOC%29%22">Skeletal Dysplasia Multidisciplinary Team (GM-MOC)</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101266602%22">Orphanet journal of rare diseases</searchLink> [Orphanet J Rare Dis] 2026 Jan 29; Vol. 21 (1). <i>Date of Electronic Publication: </i>2026 Jan 29. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22BioMed+Central%22">BioMed Central </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101266602 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1750-1172 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2217501172%22">17501172 </searchLink><i>NLM ISO Abbreviation: </i>Orphanet J Rare Dis <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=41612394 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13023-026-04219-3 Languages: – Code: eng Text: English Titles: – TitleFull: Foramen magnum stenosis, cervicomedullary decompression, and growth in children with achondroplasia: a retrospective cohort study. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Fava D – PersonEntity: Name: NameFull: Angelelli A – PersonEntity: Name: NameFull: Tedesco C – PersonEntity: Name: NameFull: Panciroli M – PersonEntity: Name: NameFull: Bianchin S – PersonEntity: Name: NameFull: Teruzzi D – PersonEntity: Name: NameFull: Scaravilli A – PersonEntity: Name: NameFull: Pisati A – PersonEntity: Name: NameFull: Barranca I – PersonEntity: Name: NameFull: Scilipoti M – PersonEntity: Name: NameFull: Severino M – PersonEntity: Name: NameFull: Napoli F – PersonEntity: Name: NameFull: Maiorano NG – PersonEntity: Name: NameFull: Naim A – PersonEntity: Name: NameFull: Negri S – PersonEntity: Name: NameFull: Patti G – PersonEntity: Name: NameFull: Pistorio A – PersonEntity: Name: NameFull: Di Iorgi N – PersonEntity: Name: NameFull: Allegri AEM – PersonEntity: Name: NameFull: Maghnie M IsPartOfRelationships: – BibEntity: Dates: – D: 29 M: 01 Text: 2026 Jan 29 Type: published Y: 2026 Identifiers: – Type: issn-electronic Value: 1750-1172 Numbering: – Type: volume Value: 21 – Type: issue Value: 1 Titles: – TitleFull: Orphanet journal of rare diseases Type: main |
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