Evidence map›Paper›PMID 24138051›Full record

ReviewSeminars in ophthalmology

The genetic basis of incomitant strabismus: consolidation of the current knowledge of the genetic foundations of disease.

Carolyn P Graeber, David G Hunter, Elizabeth C Engle

Registry-linked trialAbstract readReview
In one paragraph

Review in Seminars in ophthalmology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03059420 (Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders), which is not on this map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 7% 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.

NCT03059420 recruitingnot on this map

Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies

TypeobservationalSponsorBoston Children's HospitalRan2004 to 2030Enrolled20,000ConditionsCongenital Fibrosis of Extraocular Muscles, Duane Retraction Syndrome, Duane Radial Ray Syndrome, Mobius Syndrome
3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Outcomes of strabismus surgery in genetically confirmed congenital fibrosis of the extraocular muscles.Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus · 2019
    Article
  13. Article
  14. Horizontal gaze palsy with progressive scoliosis: is scoliosis linked to ROBO3 mutations?Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2019
    Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. PeerJ · 2017
    Article
  20. Duane retraction syndrome: causes, effects and management strategies.Clinical ophthalmology (Auckland, N.Z.) · 2017
    Review
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

3 authors at 2 institutions in 1 country.

Carolyn P GraeberBoston Children's Hospital, Boston , Massachusetts , USA and.
David G Hunter
Elizabeth C Engle
Boston Children's Museum · USHarvard University · US

Funding

MOLECULAR BASIS OF CONGENITAL STRABISMUSR01EY012498 · NEI · CHILDREN'S HOSPITAL BOSTON · PI ENGLE, ELIZABETH C. · 1999 to 2015
$5.3M
NEI NIH HHS R01 EY012498NEI NIH HHS R01 EY12498
6 · The paper itself

Abstract

In recent years, our understanding of the genetic foundations of incomitant strabismus has grown significantly. Much new understanding has been gleaned since the concept of congenital cranial dysinnervation disorders (CCDDs) was introduced in 2002, and the genetic basis of CCDDs continues to be elucidated. In this review, we aim to provide an update of the genetic and clinical presentation of these disorders. Disorders reviewed include Duane syndrome (DS), HOXA1 and HOXB1 syndromes, Moebius syndrome, congenital fibrosis of the extraocular muscles (CFEOM), and horizontal gaze palsy with progressive scoliosis (HGPPS).

Indexed as

Congenital Cranial Dysinnervation DisordersDuane Retraction SyndromeEye Diseases, HereditaryFibrosisHomeobox A1 ProteinHomeodomain ProteinsHumansMobius SyndromeOphthalmoplegiaOphthalmoplegia, Chronic Progressive ExternalScoliosisStrabismusTranscription FactorsHomeobox A1 ProteinHomeodomain ProteinsHOXB1 homeodomain proteinTranscription Factors

Identifiers

PMID24138051
PMCPMC4098966
OpenAlexW2151286401

What OpenQuestion holds

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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.