Evidence map›Paper›PMID 36719021›Full record

ArticleYonsei medical journal2023

Refractive Errors, Retinal Findings, and Genotype of Tuberous Sclerosis Complex: A Retrospective Cohort Study.

Soyoung Ryu, Hoon-Chul Kang, Sung Chul Lee, Suk Ho Byeon, Sung Soo Kim, Christopher Seungkyu Lee

Open access · goldAbstract read
In one paragraph

Article in Yonsei medical journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 25% 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.

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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Observational
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

6 authors at 2 institutions in 1 country.

Soyoung RyuThe Institute of Vision Research, Department of Ophthalmology, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-1278-9024
Hoon-Chul KangDivision of Pediatric Neurology, Department of Pediatrics, Severance Children's Hospital, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-3659-8847
Sung Chul LeeDepartment of Ophthalmology, Konyang University Hospital, Konyang University College of Medicine, Daejeon, Korea.ORCID https://orcid.org/0000-0001-9438-2385
Suk Ho ByeonThe Institute of Vision Research, Department of Ophthalmology, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-8101-0830
Sung Soo KimThe Institute of Vision Research, Department of Ophthalmology, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-3049-9554
Christopher Seungkyu LeeThe Institute of Vision Research, Department of Ophthalmology, Yonsei University College of Medicine, Seoul, Korea. sklee219@yuhs.ac.ORCID https://orcid.org/0000-0001-5054-9470
Yonsei University · KRKonyang University · KR

Funding

National Research Foundation of Korea 2019R1A2C2002393
6 · The paper itself

Abstract

purposeTo examine the refractive errors, retinal manifestations, and genotype in tuberous sclerosis complex (TSC) patients in a Korean population. MATERIALS AND

methodsA total of 98 patients with TSC were enrolled in Severance Hospital for a retrospective cohort study. The number of retinal astrocytic hamartoma and retinal achromic patch within a patient, as well as the size, bilaterality, and morphological type were studied. In addition, the refractive status of patients and the comorbidity of intellectual disability and epilepsy were also examined.

resultsRetinal astrocytic hamartoma was found in 37 patients, and bilateral invasion was observed in 20 patients (54%). TSC1 mutation was associated with myopia (

conclusionTSC1 variant patients were more myopic, while TSC2 variant patients showed association with more extensive involvement of retinal astrocytic hamartoma.

Indexed as

EpilepsyHamartomaIntellectual DisabilityRefractive ErrorsTuberous SclerosisGenotypeHumansMutationRetrospective StudiesTuberous Sclerosis Complex 1 ProteinTuberous Sclerosis Complex 2 ProteinTumor Suppressor ProteinsTSC1 protein, humanTSC2 protein, humanTuberous Sclerosis Complex 1 ProteinTuberous Sclerosis Complex 2 ProteinTumor Suppressor ProteinsgenotypehamartomaphenotypeTuberous sclerosis

Identifiers

PMID36719021
PMCPMC9892541
OpenAlexW4317486309

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.