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]
Citations
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
Cinalli, G., Rénier, D., Sebag, G., Sainte-Rose, C., Arnaud, É., & Pierre-Kahn, A. (1995) · Journal of Neurosurgery · doi:10.3171/jns.1995.83.4.0575 · Cited by 210
Self-citationIntracranial venous sinus hypertension: cause or consequence of hydrocephalus in infants?
Sainte‐Rose, C., Lacombe, J., Pierre‐Kahn, A., Rénier, D., & Hirsch, J.-F. (1984) · Journal of neurosurgery · doi:10.3171/jns.1984.60.4.0727 · Cited by 206
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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Hydrocephalus and mental retardation in craniosynostosis
Noetzel, M. J., Marsh, J. L., Palkes, H. S., & Gado, M. H. (1985) · The Journal of Pediatrics · doi:10.1016/s0022-3476(85)80181-5 · Cited by 117
THROMBOSIS OF THE DURAL VENOUS SINUSES AS A CAUSE OF "PSEUDOTUMOR CEREBRI"*
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Cinalli, G., Chumas, P., Arnaud, É., Sainte‐Rose, C., & Rénier, D. (1998) · Neurosurgery · doi:10.1097/00006123-199801000-00013 · Cited by 93
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
Self-citation
Research works printed but not linked: 3
- Cinalli G, Neurosurgery
- Marchac D, 1979, Ann Chir Plast, 24, 121
- Pierre-Kahn A, 1980, Childs Brain, 7, 205
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Chiari malformation in craniosynostosis
Cinalli, G., Spennato, P., Sainte-Rose, C., Arnaud, É., Aliberti, F., Brunelle, F., Cianciulli, E., & Rénier, D. (2005) · Child's Nervous System · doi:10.1007/s00381-004-1115-z · Cited by 253
Self-citationMathijssen, I. M. J. (2015) · Journal of Craniofacial Surgery · doi:10.1097/scs.0000000000002016 · Cited by 232
Hydrocephalus in craniosynostosis: a review
Collmann, H., Sörensen, N., & Krauß, J. (2005) · Child s Nervous System · doi:10.1007/s00381-004-1116-y · Cited by 192
A morphometric analysis of the foramen magnum region as it relates to the transcondylar approach
Muthukumar, N., Swaminathan, R., Venkatesh, G., & Bhanumathy, S. P. (2005) · Acta Neurochirurgica · doi:10.1007/s00701-005-0555-x · Cited by 167
Craniopharyngioma: modern concepts in pathogenesis and treatment
Garrè, M. L., & Cama, A. (2007) · Current Opinion in Pediatrics · doi:10.1097/mop.0b013e3282495a22 · Cited by 164
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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