The DOI matches its Crossref record; 30 of the 30 references it cites were found in a registry or an index.
Hydrocephalus and craniosynostosis
Abstract
OBJECT: A retrospective study of 1727 cases of craniosynostosis was undertaken to determine the interrelationship between abnormal cerebrospinal fluid (CSF) hydrodynamics and craniosynostosis. METHODS: The patients were divided into two groups: nonsyndromic craniosynostosis and syndromic craniosynostosis. Cases of occipital plagiocephaly without suture synostosis and cases of shunt-induced craniosynostosis were excluded from the study. The majority of patients (1297) were treated surgically for their cranial deformity; 95% of these patients had a postoperative follow-up review period lasting 5 years. Clinical and radiographic charts covering the time from presentation through the follow-up period were reviewed. CONCLUSIONS: Abnormal intracranial CSF hydrodynamics was found in 8.1% of the patients (3.4% of whom had received shunts and 4.5% of whom had not). Three types of CSF hydrodynamic disturbance were observed: progressive hydrocephalus with ventricular dilation, nonprogressive ventriculomegaly, and dilation of the subarachnoid spaces. Hydrocephalus occurred much more frequently in patients with syndromic craniosynostosis (12.1%) than in those with isolated craniosynostosis (0.3%). In fact, patients with kleeblattschädel exhibited hydrocephalus as a constant feature and patients with Crouzon's syndrome were far more likely to have hydrocephalus than those with other syndromes. In Apert's syndrome, ventricular dilation occurred very frequently, but it was almost always nonprogressive in nature. In most cases of syndromic craniosynostosis, venous sinus obstruction and/or chronic tonsillar herniation were found. Their role in the pathophysiology of hydrocephalus in craniosynostosis is discussed.
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“It occurs more frequently in boys than in girls.”
From Isolated Sagittal Craniosynostosis: A Comprehensive Review (2024) · cites this paper as [4]
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Cites
Intracranial pressure in craniostenosis
Renier, D., Sainte-Rose, C., Marchac, D., & Hirsch, J.-F. (1982) · Journal of neurosurgery · doi:10.3171/jns.1982.57.3.0370 · Cited by 591 · cited 2×
“The association between hydrocephalus and craniosynostosis has been well documented and the incidence of hydrocephalus has been found to be between 4% and 10%.[6-9,15,16,18,23,25,26,28] A significant”
BackgroundSelf-citationEpidemiology of Cerebrospinal Fluid Shunting
Bondurant, C. P., & Jimenez, D. F. (2008) · Pediatric Neurosurgery · doi:10.1159/000120968 · Cited by 288
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Self-citationIntracranial venous sinus hypertension: cause or consequence of hydrocephalus in infants?
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Self-citationPrognosis for mental function in Apert's syndrome
Rénier, D., Arnaud, É., Cinalli, G., Sebag, G. H., Zérah, M., & Marchac, D. (1996) · Journal of neurosurgery · doi:10.3171/jns.1996.85.1.0066 · Cited by 190
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Self-citationClassification of previously unclassified cases of craniosynostosis
Chumas, P., Cinalli, G., Arnaud, É., Marchac, D., & Rénier, D. (1997) · Journal of neurosurgery · doi:10.3171/jns.1997.86.2.0177 · Cited by 92
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- Cinalli G, Neurosurgery
- Marchac D, 1979, Ann Chir Plast, 24, 121
- Pierre-Kahn A, 1980, Childs Brain, 7, 205
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Items 201–224 of 224
Acquired hump of the corpus callosum: a rare morphologic complication after CSF shunting
Simsek, O., Alves, C., & Andronikou, S. (2023) · Child s Nervous System · doi:10.1007/s00381-023-05875-7
MR Protocols for Paediatric Neurosurgical Common Conditions: An Update Guide for Neurosurgeons
Vito, A. D., Zvi, I. B., & D’Arco, F. (2023) · Advances and technical standards in neurosurgery · doi:10.1007/978-3-031-36785-4_3
Cinalli, G., Scala, M. R., & Aliberti, F. (2023) · Springer eBooks · doi:10.1007/978-3-031-47681-5_4
Self-citationJung, J., Lam, J., deSouza, R., Anderson, I., & Chumas, P. (2019) · Advances in Clinical Neuroscience & Rehabilitation · doi:10.47795/vdbt8588
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Rodriguez-Verduzco, J., Resendiz-Olascoaga, A., Pacheco-Ruiz, S., Mancilla-Hernández, F., Gonzalez-Macedo, J., Correa-Castillo, M., Alaniz-Arellano, J., & Rosas, D. M. S. (2024) · Revista Internacional de Salud Materno Fetal · doi:10.47784/rismf.2023.8.4.322
Pontell, M. E., Barrero, C. E., Naidu, K., Hitchner, M. K., Wagner, C. S., Salinero, L. K., Swanson, J. W., Bartlett, S. P. P., & Taylor, J. A. (2024) · Journal of Craniofacial Surgery · doi:10.1097/scs.0000000000010405
Free-floating bone flap posterior cranial vault release in syndromic craniosynostosis
Liang, Q., Kang, X., Gao, P., Xia, Z.-Y., Sun, Y., & Bao, N. (2024) · Journal of Cranio-Maxillofacial Surgery · doi:10.1016/j.jcms.2024.11.009
Hydrocephalus and Craniosynostosis
Schulz, M., & Thomale, U. (2024) · Springer eBooks · doi:10.1007/978-3-031-69386-1_35
Nadel, J., & Kestle, J. R. W. (2024) · Springer eBooks · doi:10.1007/978-3-031-69386-1_16
Multiple Sutures Synostosis: Key Points for the Neurosurgeons and Management Principles
Swift, D. M. (2024) · Springer eBooks · doi:10.1007/978-3-031-69386-1_13
Venous Anomalies in Craniosynostosis
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Ventricular and Pericerebral Cerebrospinal Fluid Accumulation in Craniosynostosis
Rocco, F. D. (2024) · Springer eBooks · doi:10.1007/978-3-031-69386-1_15
Mena-Bernal, J. H., & Castro, M. V. B. (2024) · Springer eBooks · doi:10.1007/978-3-031-69386-1_12
Management of Hydrocephalus in Patients with Craniosynostosis
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Complex Head Reconstruction in Syndromic Craniosynostosis Patients
Meyer, U., Hoffmann, B., & Schick, U. (2024) · Springer eBooks · doi:10.1007/978-3-031-51773-0_4
Surgical Management of Syringomyelia with Craniosynostosis
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Modern concepts of CSF disorders in monosutural craniosynostosis
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D, G. P. M., Protzenko, T., Khonsari, R. H., James, S., & Arnaud, É. (2026) · Springer eBooks · doi:10.1007/978-3-032-12551-4_14
Neurocognitive Implications, Etiological Mechanisms, and Clinical Care Recommendations
Costa, A. C. D., & Kapp‐Simon, K. A. (2026) · Springer eBooks · doi:10.1007/978-3-032-12551-4_33
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Glaeser-Khan, S., Salib, A., Allen, G., Kong, V., Moscarelli, J. R., Singh, N., Rindani, M., Lewis, K., Allam, O., & Alperovich, M. A. (2026) · The Cleft Palate-Craniofacial Journal · doi:10.1177/10556656261483537
Bicoronal and Multisuture Craniosynostosis
Hollier, P. C., Quirarte, D. M., Burns, H. R., & Monson, L. A. (2026) · Seminars in Plastic Surgery · doi:10.1055/a-2942-5505
Metadata
- Authors
- Cinalli, G., Sainte-Rose, C., Kollar, E. M., Zerah, M., Brunelle, F., Chumas, P., Arnaud, E., Marchac, D., Pierre-Kahn, A., & Renier, D.
- Affiliations
- Hôpital Necker-Enfants Malades (FR)
- Venue
- Journal of neurosurgery
- Published
- 1998-02
- Volume
- 88
- Issue
- 2
- Pages
- 209-214
- ISSN
- 0022-3085 (ISSN-L)
- OpenAlex
- W2155932531
- Cited by
- 224
- References
- 30
- Citations by year
- 2026: 7 · 2025: 6 · 2024: 22 · 2023: 11 · 2022: 12 · 2021: 17 · 2020: 11 · 2019: 21 · 2018: 11 · 2017: 15 · 2016: 7 · 2015: 8 · 2014: 2 · 2013: 5 · 2012: 11
- FWCI
- 1.33
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of neurosurgery (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Surgery › Craniofacial Disorders and Treatments
- Health Sciences › Medicine › Clinical Neurology › Cerebrospinal fluid and hydrocephalus
- Health Sciences › Medicine › Clinical Neurology › Spinal Dysraphism and Malformations
- Keywords
- craniosynostosis, hydrocephalus, cerebrospinal fluid dynamics, syndromic craniosynostosis, nonsyndromic craniosynostosis, ventriculomegaly, Crouzon syndrome, Apert syndrome, cerebellar tonsil herniation, cranial deformity surgery
- MeSH terms
- Acrocephalosyndactylia, Brain, Child, Preschool, Craniofacial Dysostosis, Craniosynostoses, Humans, Hydrocephalus, Infant, Retrospective Studies, Syndrome, Tomography, X-Ray Computed, Disease Progression
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