Evidence map›Paper›PMID 37894926›Full record

ArticleInternational journal of molecular sciences2023

Prevalence of Congenital Color Vision Deficiency in Southern Taiwan and Detection of Female Carriers by Visual Pigment Gene Analysis.

Hsi-Kung Kuo, Shih-Ting Tsao, Pei-Chang Wu

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 40% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Factors affecting color vision: a systematic review.International journal of ophthalmology · 2026
    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.

Hsi-Kung KuoDepartment of Ophthalmology, Kaohsiung Chang-Gung Memorial Hospital, Kaohsiung 833, Taiwan.
Shih-Ting TsaoDepartment of Ophthalmology, Kaohsiung Chang-Gung Memorial Hospital, Kaohsiung 833, Taiwan.
Pei-Chang WuDepartment of Ophthalmology, Kaohsiung Chang-Gung Memorial Hospital, Kaohsiung 833, Taiwan.ORCID 0000-0002-7201-1900
Chang Gung University · TWKaohsiung Chang Gung Memorial Hospital · TW

Funding

Kaohsiung Chang-Gung Memorial Hospital, Taiwan CMRPG8J1531
6 · The paper itself

Abstract

This study aimed to investigate the prevalence of color vision deficiencies (CVDs) and determine whether carriers could be detected by analyzing the visual pigment genes. Materials and Methods: The data of students who underwent routine CVD screening using the Ishihara color test in Kaohsiung, Southern Taiwan were analyzed. Furthermore, the DNA samples of 80 randomly selected females and four obligate carriers were analyzed. The most upstream genes, downstream genes, and the most downstream genes in the red/green pigment gene arrays were amplified separately using polymerase chain reaction (PCR), and exon 5 of each gene was analyzed. The prevalence of congenital red-green CVD in this study was 3.46% in males and 0.14% in females. The PCR analysis of the first gene, downstream gene, and last gene revealed normal patterns in 73 normal cases. Seven unusual patterns were detected in two proton carriers and five deutan carriers. Among the randomly selected females, 8.8% (7/80) were CVD carriers. The prevalence of CVD among male Taiwanese students in this study was 3.46%. Female carriers of congenital CVD can be identified by molecular analysis of the visual pigment genes. The proportion of CVD carriers among the randomly selected females was 8.8%, which was slightly higher than expected and further studies are warranted.

Indexed as

Cardiovascular DiseasesColor Vision DefectsColor PerceptionFemaleHumansMalePrevalenceRetinal PigmentsTaiwanRetinal Pigmentscolor vision deficienciesdeutan carrierpolymerase chain reactionprevalenceproton carriervisual pigment genes

Identifiers

PMID37894926
PMCPMC10607166
OpenAlexW4387705536

What OpenQuestion holds

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LicenceCC BY
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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.