Evidence map›Paper›PMID 18925666›Full record

ArticleAmerican journal of medical genetics. Part A2008

Neuroimaging aspects of Aicardi syndrome.

Bobbi Hopkins, V Reid Sutton, Richard Alan Lewis, Ignatia Van den Veyver, Gary Clark

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in American journal of medical genetics. Part A, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00697411 (Pathogenesis of Selected X-Linked Dominant Disorders and New Strategies to Identify the Gene Mutated in Aicardi Syndrome), which is not on this map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
7.0field-weighted citation impact, top 4% of its field
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.

NCT00697411 recruitingnot on this map

Pathogenesis of Selected X-Linked Dominant Disorders and New Strategies to Identify the Gene Mutated in Aicardi Syndrome

TypeobservationalSponsorBaylor College of MedicineRan2002 to 2030Enrolled500ConditionsAicardi Syndrome, Brain DisordersArmsSyndrome cause identification
3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 84 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Imaging of fetal brain tumors.Pediatric radiology · 2020
    Review
  11. Article
  12. Foetal Magnetic Resonance Images of Two Cases of Aicardi Syndrome.Journal of clinical and diagnostic research : JCDR · 2017
    Article
  13. Independent variant analysis ofMolecular genetics & genomic medicine · 2017
    Article
  14. Review
  15. Article
  16. Review
  17. Palliative epilepsy surgery in Aicardi syndrome: a case series and review of literature.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2014
    Article
  18. Article
  19. Article
  20. Article
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

5 authors at 1 institution in 1 country.

Bobbi HopkinsDepartment of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA.
V Reid Sutton
Richard Alan Lewis
Ignatia Van den Veyver
Gary Clark
Baylor College of Medicine · US

Funding

UNDERSTANDING FXTAS AMONG MALES WITH THE FMR1 PREMUTATIONP30HD024064 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI TOLIAS, KIMBERLY R · 1988 to 2013
$29.4M
New strategies to identify the gene mutated in Aicardi syndromeR21HD051805 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI VAN DEN VEYVER, IGNATIA B · 2007 to 2008
$409k
NICHD NIH HHS HD024064NICHD NIH HHS P30 HD024064NICHD NIH HHS R21 HD051805
6 · The paper itself

Abstract

Aicardi syndrome is a rare neurodevelopmental disorder characterized by congenital chorioretinal lacunae, corpus callosum dysgenesis, seizures, polymicrogyria, cerebral heterotopias, intracranial cysts, and costovertebral defects. Cerebellar abnormalities have been described occasionally. Aicardi syndrome is sporadic and has been observed only in females and 47,XXY males. Therefore, it is thought to result from a mutation in an X-linked gene. Improved definition of the clinical phenotype should focus the selection of functional candidate genes for mutation analysis. Because central nervous system abnormalities are the most prominent component of the phenotype, we performed a detailed characterization of abnormalities identified on magnetic resonance neuroimaging studies from 23 girls with Aicardi syndrome, the largest cohort to undergo such review by a single group of investigators. All patients had polymicrogyria that was predominantly frontal and perisylvian and often associated with underopercularization. Periventricular nodular heterotopias, present in all patients, were more frequent than previously reported; 10 had single and 11 had multiple intracranial cysts. Posterior fossa abnormalities were also more frequent than previously described. Cerebellar abnormalities were noted in 95% of studies where they could be evaluated. As a novel finding, we noted tectal enlargement in 10 patients. Since mildly affected girls with variable callosal dysgenesis have now been reported, the constellation of frontal-dominant and perisylvian polymicrogyria, periventricular nodular heterotopias, intracranial cysts, and posterior fossa abnormalities, including tectal enlargement, should prompt consideration of the diagnosis of Aicardi syndrome. We further propose that improved characterization of the neurological phenotype will benefit the selection of candidate genes for mutation analysis.

Indexed as

Abnormalities, MultipleBrainCentral Nervous System CystsCerebellumChildChild, PreschoolFemaleHumansInfantInfant, NewbornMagnetic Resonance ImagingMaleMalformations of Cortical DevelopmentPeriventricular Nodular HeterotopiaSyndrome

Identifiers

PMID18925666
PMCPMC2597151
OpenAlexW2113746873

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.