Bianca K. den Ottelander
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View article: Quantitative Detection and Follow-Up of Intracranial Hypertension in Craniosynostosis: An Optical Coherence Tomography Study
Quantitative Detection and Follow-Up of Intracranial Hypertension in Craniosynostosis: An Optical Coherence Tomography Study Open
Background: In patients with craniosynostosis, the authors evaluated the diagnostic accuracy of fundoscopy and optical coherence tomography (OCT) to detect intracranial hypertension (ICH), the time course of retinal thickness after treatme…
View article: The use of OCT to detect signs of intracranial hypertension in patients with sagittal suture synostosis: Reference values and correlations
The use of OCT to detect signs of intracranial hypertension in patients with sagittal suture synostosis: Reference values and correlations Open
Purpose To obtain pediatric normative reference values and determine whether optical coherence tomography (OCT) corresponds better with clinical signs of intracranial hypertension (ICH) compared to the traditional screening method fundosco…
View article: Quantified Retinal Morphology and Its Association With Papilledema and Visual Acuity in Syndromic and Complex Craniosynostosis: An Optical Coherence Tomography Study
Quantified Retinal Morphology and Its Association With Papilledema and Visual Acuity in Syndromic and Complex Craniosynostosis: An Optical Coherence Tomography Study Open
Following a preventative treatment strategy for syndromic and complex craniosynostosis, the prevalence of retinal ONH thinning is low. Although the prevalence of peripapillary retinal nerve fiber layer thinning is considerable, its thickne…
View article: Cerebral cortex maldevelopment in syndromic craniosynostosis
Cerebral cortex maldevelopment in syndromic craniosynostosis Open
Aim To assess the relationship of surface area of the cerebral cortex to intracranial volume (ICV) in syndromic craniosynostosis. Method Records of 140 patients (64 males, 76 females; mean age 8y 6mo [SD 5y 6mo], range 1y 2mo–24y 2mo) with…
View article: Cervical Spinal Cord Compression and Sleep-Disordered Breathing in Syndromic Craniosynostosis
Cervical Spinal Cord Compression and Sleep-Disordered Breathing in Syndromic Craniosynostosis Open
The prevalence of cervical spinal cord compression in syndromic craniosynostosis is low and is not correlated to sleep disturbances. However, considering the high prevalence of obstructive sleep apnea in syndromic craniosynostosis and the …
View article: Saethre–Chotzen syndrome: long‐term outcome of a syndrome‐specific management protocol
Saethre–Chotzen syndrome: long‐term outcome of a syndrome‐specific management protocol Open
Aim To assess the long‐term outcomes of our management protocol for Saethre–Chotzen syndrome, which includes one‐stage fronto‐orbital advancement. Method All patients born with Saethre–Chotzen syndrome between January 1992 and March 2017 w…
View article: Dural sinus volume in children with syndromic craniosynostosis and intracranial hypertension
Dural sinus volume in children with syndromic craniosynostosis and intracranial hypertension Open
OBJECTIVE Intracranial hypertension is a major concern in children with syndromic craniosynostosis (sCS). Cerebral venous hypertension caused by cerebral venous outflow obstruction is believed to contribute to intracranial hypertension. Th…
View article: Intracranial hypertension and cortical thickness in syndromic craniosynostosis
Intracranial hypertension and cortical thickness in syndromic craniosynostosis Open
Aim To evaluate the impact of risk factors for intracranial hypertension (ICH) on cerebral cortex thickness in syndromic craniosynostosis. Method ICH risk factors including papilloedema, hydrocephalus, obstructive sleep apnea (OSA), cerebe…
View article: Cerebral blood flow in children with syndromic craniosynostosis: cohort arterial spin labeling studies
Cerebral blood flow in children with syndromic craniosynostosis: cohort arterial spin labeling studies Open
OBJECTIVE In comparison with the general population, children with syndromic craniosynostosis (sCS) have abnormal cerebral venous anatomy and are more likely to develop intracranial hypertension. To date, little is known about the postnata…
View article: Improvement in Sleep Architecture is associated with the Indication of Surgery in Syndromic Craniosynostosis
Improvement in Sleep Architecture is associated with the Indication of Surgery in Syndromic Craniosynostosis Open
Background: Children with syndromic craniosynostosis (sCS) often suffer from obstructive sleep apnea (OSA) and intracranial hypertension (ICH). Both OSA and ICH might disrupt sleep architecture. However, it is unclear how surgically treati…
View article: S1-02 SESSION 1: NEUROSURGERY INTRACRANIAL HYPERTENSION AND CORTICAL THICKNESS IN SYNDROMIC CRANIOSYNOSTOSIS
S1-02 SESSION 1: NEUROSURGERY INTRACRANIAL HYPERTENSION AND CORTICAL THICKNESS IN SYNDROMIC CRANIOSYNOSTOSIS Open
Introduction: Intracranial hypertension (ICH) is a frequent indication for surgical intervention in syndromic craniosynostosis. Various clinical risk factors have been described, but potential effects on underlying brain morphology have no…
View article: S6A-09 SESSION 6A: CORONAL SYNOSTOSIS MUENKE SYNDROME: LONG-TERM OUTCOME OF A SYNDROME-SPECIFIC TREATMENT PROTOCOL
S6A-09 SESSION 6A: CORONAL SYNOSTOSIS MUENKE SYNDROME: LONG-TERM OUTCOME OF A SYNDROME-SPECIFIC TREATMENT PROTOCOL Open
Introduction: To evaluate the long-term outcome of our treatment protocol for Muenke syndrome, consisting of a single craniofacial procedure. Methods: Prospective observational cohort study of Muenke syndrome patients who underwent surgery…
View article: Intracranial Hypertension and Cortical Thickness in Syndromic Craniosynostosis
Intracranial Hypertension and Cortical Thickness in Syndromic Craniosynostosis Open
INTRODUCTION: Intracranial hypertension (ICH) is a frequent indication for surgical intervention in syndromic craniosynostosis. Various clinical risk factors have been described, but potential effects on underlying brain morphology have no…
View article: S14-03 SESSION 14: FACIOCRANIOSYNOSTOSIS – PART III SAETHRE-CHOTZEN SYNDROME: LONG-TERM OUTCOME OF A SYNDROME-SPECIFIC TREATMENT PROTOCOL
S14-03 SESSION 14: FACIOCRANIOSYNOSTOSIS – PART III SAETHRE-CHOTZEN SYNDROME: LONG-TERM OUTCOME OF A SYNDROME-SPECIFIC TREATMENT PROTOCOL Open
Introduction: To assess the long-term outcomes of our standard treatment protocol for Saethre-Chotzen syndrome (SCS), which includes one-stage fronto-orbital advancement (FOA). Methods: We included all patients born with SCS between Jan 19…
View article: S8A-12 SESSION 8A: METOPIC SYNOSTOSIS OPHTHALMOLOGIC ABNORMALITIES IN CHILDREN WITH TRIGONOCEPHALY
S8A-12 SESSION 8A: METOPIC SYNOSTOSIS OPHTHALMOLOGIC ABNORMALITIES IN CHILDREN WITH TRIGONOCEPHALY Open
Introduction: Little has been described in the literature regarding ophthalmic abnormalities in non-syndromic midline craniosynostosis. The few studies on non-syndromic trigonocephaly and ocular abnormalities have shown that non-syndromic …