Evidence map›Paper›PMID 42754594›Full record

ReviewNature reviews. Disease primers2026

Chiari I malformation.

Andrew T Hale, Douglas L Brockmeyer, William C Davalan, A Graham Fieggen, Gerald A Grant, Eric M Jackson, Adam J Kundishora, David D Limbrick, Cormac O Maher, Brandon G Rocque and 4 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Disease primers, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Andrew T HaleDepartment of Neurosurgery, University of Alabama at Birmingham, Birmingham, AL, USA.ORCID http://orcid.org/0000-0003-3182-2966
Douglas L BrockmeyerDepartment of Neurosurgery, University of Utah, Salt Lake City, UT, USA.
William C DavalanDepartment of Neurosurgery, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
A Graham FieggenNeuroscience Institute, University of Cape Town, Cape Town, South Africa.
Gerald A GrantDepartment of Neurosurgery, Duke University School of Medicine, Durham, NC, USA.
Eric M JacksonDepartment of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Adam J KundishoraDivision of Neurosurgery, Children's Hospital of Philadelphia, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0001-6419-7955
David D LimbrickDepartment of Neurosurgery, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
Cormac O MaherDepartment of Neurosurgery, Stanford University School of Medicine, Palo Alto, CA, USA.
Brandon G RocqueDepartment of Neurosurgery, University of Alabama at Birmingham, Birmingham, AL, USA.
Jennifer M StrahleDepartment of Neurosurgery, Washington University in St. Louis, St. Louis, MO, USA.
Dominic M ThompsonDepartment of Neurosurgery, Great Ormond Street Hospital, London, UK.
Alexander M TuckerDivision of Neurosurgery, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Kristopher T KahleDepartment of Neurosurgery, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA. kahle.kristopher@mgh.harvard.edu.ORCID http://orcid.org/0000-0002-5922-7547

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chiari I malformation (CM1), the most common structural hindbrain disorder in humans, is traditionally characterized by the downward displacement of the cerebellar tonsils through the foramen magnum. However, this definition does not reflect the variability in clinical presentation, natural history and treatment response of this disorder. Some individuals with minimal tonsillar descent have severe neurological symptoms and syringomyelia, whereas others with extensive descent remain asymptomatic. Emerging evidence from neuroimaging, developmental biology and human genetics indicates that CM1 is not a single anatomical entity but a spectrum of disorders resulting from disruptions in coordinated growth and homeostasis across the cerebellum, posterior fossa, craniocervical junction, cerebrospinal fluid and neurovascular systems. CM1 may be best understood as a disorder of disrupted developmental scaling, in which the tightly regulated relationships between cerebellar growth and cranial accommodation are altered within a dynamic neurovascular and cerebrospinal fluid environment. In this context, tonsillar herniation is a geometric consequence rather than the primary disease process. This Primer synthesizes current knowledge on the epidemiology, mechanisms, diagnosis and management of CM1 across the lifespan. We highlight advances in neuroimaging, genomics and phenomics that support a shift from anatomy-based definitions towards an integrated genomic-phenomic classification.

Indexed as

Arnold-Chiari MalformationCerebellumHumansMagnetic Resonance ImagingNeuroimaging

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.