ReviewChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2019
Clinical diagnosis-part I: what is really caused by Chiari I.
Review in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.
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19 citing papers in PubMed, 36 citations in OpenAlex.
- Clinical and MRI morphometric characterization of symptomatic cerebellar tonsillar ectopia.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026Article
- Central hypoventilation and choking episodes revealing Chiari malformation type I.BMJ case reports · 2026Article
- Paediatric isolated foot drop-a rare presentation of Chiari 1 malformation with holocord syrinx (case report and the review of literature).Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2025Review
- Measurement of CSF flow and brain motion in Chiari malformation type I subjects undergoing posterior fossa decompression surgery.Journal of neurosurgery · 2025Article
- Hyponatremia Presents With Seizure in a Patient With Arnold-Chiari Malformation: A Case Report.Cureus · 2025Article
- Article
- Utilization of Vestibular Information for Balance Control in Children with Chiari I Malformation.Audiology research · 2024Article
- Clinical analysis of atlanto-occipital decompression in the management of chiari malformation with multi-segmental syringomyelia.Frontiers in pediatrics · 2024Article
- The Small Posterior Cranial Fossa Syndrome and Chiari Malformation Type 0.Journal of clinical medicine · 2022Review
- Neurophysiological Correlates in Patients with Syringomyelia and Chiari Malformation: The Cortico-Diaphragmatic Involvement.Journal of clinical medicine · 2022Article
- Migraine in Chiari 1 Malformation: a cross-sectional, single centre study.Acta neurologica Belgica · 2022Article
- Chiari malformation type 1 presenting as isolated unilateral foot drop with rapid recovery following posterior fossa decompression.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2022Review
- Diagnosis and treatment of Chiari malformation type 1 in children: the International Consensus Document.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022Article
- Diagnosis and treatment of Chiari malformation and syringomyelia in adults: international consensus document.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022Article
- Increase in clivo-axial angle is associated with clinical improvement in children undergoing occipitocervical fusion for complex Chiari malformation: patient series.Journal of neurosurgery. Case lessons · 2021Article
- Preoperative measurements on MRI in Chiari 1 patients fail to predict outcome after decompressive surgery.Acta neurochirurgica · 2021Article
- Natural history of Chiari I malformation in children: a retrospective analysis.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021Article
- Long-term outcomes for children with an incidentally discovered Chiari malformation type 1: what is the clinical significance?Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021Article
- Chiari malformation type 1: are we doing less with more? Illustrative case.Journal of neurosurgery. Case lessons · 2021Article
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4 authors at 2 institutions in 1 country.
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Abstract
purposeChiari malformation is a group of congenital malformations involving the brainstem, cerebellum, and upper spinal cord, frequently identified in both young adults and in children. Chiari I malformation (CM1), classically defined as a caudal displacement of the cerebellar tonsils through the foramen magnum into the spinal cord, is the most common clinical type. A syringomyelia can be associated at the time of the diagnosis or appear secondarily and manifest with medullary symptoms. The aim of this paper is to update the knowledge on clinical manifestations specifically related to Chiari I malformation with or without syringomyelia in the pediatric population.
methodsCurrent literature with focus on relevant clinical pediatric issues is reviewed and discussed, comparing with those related to adults; we include the results of a 10-year single-center experience on 600 CM1 patients. RESULTS AND
conclusionsHerniation of the cerebellar tonsils may lead to significant clinical symptoms, including neck and cervical pain, short-lasting occipital "cough" headache, dizziness, and gait impairment; in children younger than 3 years, oropharyngeal symptoms are prevalent (sleep apnea, feeding problems) whereas in those older than 3 years, a higher incidence of cough headache and scoliosis is reported. CM1 clinical features, both in children and in adults, have in common the presence of anatomical deformities of the brainstem and cerebellum. Clinical myelopathy (sensory/autonomic disorders, motor weakness) can result from direct compression of the cervical spinal cord by the herniated cerebellar tonsils or can be due to the presence of a syrinx, reported in association with Chiari I between 35 and 75% of pediatric patients. Similarly, in our series (440 females, 160 males, 98% > 18 years), syringomyelia associated with Chiari I was ranging from 40 to 60% (respectively in asymptomatic and symptomatic groups); headache was reported in 65%. Sensory disturbances (48%), cranial nerve deficits (45%), motor weakness (32%), and autonomic disorders (35%) were the most frequent neurological signs in our cohort. In Chiari I malformation, cervical pain and occipital cough headache are the most characteristic presenting symptoms, both in old children and in adults; however, headache is often multifactorial, and CM1 patients can report a wide variety of non-specific symptoms and signs. Clinical diagnostic CM1 criteria, shared at the national and international level, are recommended with the aim to avoid consequent controversies on diagnosis and on surgical decision making.
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