Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A genetic hypothesis for Chiari I malformation with or without syringomyelia.

Neurosurgical focus - 15 Mar 2000

Speer M C, George T M, Enterline D S, Franklin A, Wolpert C M, Milhorat T H

Abstract excerpt

In several reports the authors have suggested occasional familial aggregation of syringomyelia and/or Chiari 1 malformation (CM1). Familial aggregation is one characteristic of traits that have an underlying genetic basis. The authors provide evidence for familial aggregation of CM1 and syringomyelia (CM1/S) in a large series of families, establishing that there may be a genetic component to CM1/S in at least a...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Congenital Anomalies and Fetal Surgery
Share to Congenital Diaphragmatic Hernia Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Spinal Dysraphism and Malformations

Source

Identifiers

PMID: 16676924
DOI: 10.3171/foc.2000.8.3.12

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A genetic hypothesis for Chiari I malformation with or without syringomyelia.PMID 16676924Read ↗

Review Article: Chiari Type I Malformation with or Without Syringomyelia: Prevalence and GeneticsSemantic proximity Read ↗

Phenotypes and prognostic factors of syringomyelia in single-center patients with Chiari I malformation: moniliform type as a special configurationSemantic proximity Read ↗

Evidence of Posterior Fossa Hypoplasia in the Familial Variant of Adult Chiari I Malformation: Case ReportSemantic proximity Read ↗

Noonan syndrome and type 1 Chiari malformation: Possible association.Semantic proximity Read ↗

Syringomyelia and Chiari Syndrome Registry: advances in epidemiology, clinical phenotypes and natural history based on a North Western Italy cohort.Semantic proximity Read ↗

Population-based description of familial clustering of Chiari malformation Type I.Semantic proximity Read ↗

Idiopathic scoliosis as a presenting sign of familial neurologic abnormalities.Semantic proximity Read ↗

[Chiari-like malformation--syringomyelia in the Cavalier King Charles Spaniel].Semantic proximity Read ↗

Holocord syringomyelia as the dominant feature in Noonan's syndrome.Semantic proximity Read ↗

[Hemihypertrophy and scoliosis revealing a Chiari 1 malformation with syringomyelia].Semantic proximity Read ↗

An additional case of cerebrofaciothoracic dysplasia associated with Chiari type I malformation.Semantic proximity Read ↗

Hypothesis on the pathophysiology of syringomyelia based on analysis of phase-contrast magnetic resonance imaging of Chiari-I malformation patientsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.