The management of Chiari malformation type 1 and syringomyelia in children: a review of the literature

V Saletti, M Farinotti, P Peretta, L Massimi… - Neurological …, 2021 - Springer
In anticipation of the “Chiari and Syringomyelia Consensus Conference” held in Milan in
2019, we performed a systematic literature review on the management of Chiari …

Role of sleep study in children with Chiari malformation and sleep disordered breathing

F Abel, MZ Tahir - Child's Nervous System, 2019 - Springer
Purpose Chiari malformation incorporate numerous forms of congenital or acquired
cerebellar herniation through the foramen magnum. This may lead to brain stem, high spinal …

Chiari 1 malformation and untreated sagittal synostosis: a new subset of complex Chiari?

LG Valentini, V Saletti, A Erbetta, L Chiapparini… - Child's Nervous …, 2019 - Springer
Abstract Purpose Chiari 1 malformation (CM1) is a well-known association with complex
craniosynostosis (CC), while it has been rarely reported in association with monosynostosis …

Craniosynostosis is a feature of Costello syndrome

KN Weaver, M Care, E Wakefield… - American Journal of …, 2022 - Wiley Online Library
Costello syndrome (CS) is an autosomal dominant disorder caused by pathogenic variants
in HRAS. Craniosynostosis is a known feature of other RASopathies (Noonan and …

Endoscopic third ventriculostomy for hydrocephalus after craniovertebral decompression for Chiari malformation type I: technical nuances and surgical pitfalls

J Pepper, D Rodrigues, P Gallo - Child's Nervous System, 2023 - Springer
Purpose Hydrocephalus after craniovertebral decompression (CVD) for Chiari I
malformation (CM-1) is a well-recognised complication. The mainstay of management …

Cerebellar Tonsils Herniation and Syringomyelia in Craniosynostoses

L Massimi - Neurosurgical Aspects of Craniosynostosis, 2025 - Springer
The anatomy and the morfo-volumetric analysis of the posterior fossa currently raise a great
interest among physicians due to the increasing number of diagnosis of Chiari I …

Surgical outcomes of calvaria reconstruction in cranial pansynostosis associated with Arnold‐Chiari type 1.5 malformation, a case report

H Tabesh, A Riazi, M Mahmoodkhani… - Clinical Case …, 2023 - Wiley Online Library
A 6‐year‐old girl with persistent headaches and the visual problem was diagnosed as a
delayed onset cranial pansynostosis with concurrent type 1.5 Arnold‐Chiari malformation …

Human genetics and molecular genomics of Chiari malformation type 1

KY Mekbib, W Muñoz, G Allington, S McGee… - Trends in Molecular …, 2023 - cell.com
Abstract Chiari malformation type 1 (CM1) is the most common structural brain disorder
involving the pboard1 junction, characterized by caudal displacement of the cerebellar …

[PDF][PDF] Turner Syndrome and Craniosynostosis: An Unusual Combination

V Becerra, J Hinojosa, M Alamar - NEUROLOGY, 2021 - emjreviews.com
This article describes a case of Turner syndrome (TS) associated with craniosynostosis due
to an early closure of the sagittal suture. Skeletal anomalies are characteristic phenotypic …

MicroRNA profiling in body fluids of patients affected by Autism Spectrum Disorder, Tourette syndrome and Arnold-Chiari syndrome

F Mirabella - 2021 - tesidottorato.depositolegale.it
The growing prevalence of neurodevelopmental disorders (NDDs) is leading to a significant
social impact and a considerable interest in the scientific community. In the last decades …