Evidence map›Paper›PMID 37915370›Full record

ArticleRespirology case reports2023

X -linked inheritance of primary ciliary dyskinesia and retinitis pigmentosa due to

Aoi Kuroda, Ho Namkoong, Eri Iwami, Akihiro Tsutsumi, Takahiro Nakajima, Hajime Shinoda, Yusaku Katada, Jiro Iimura, Hisato Suzuki, Kenjiro Kosaki and 1 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Respirology case reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 5 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Aoi KurodaDepartment of Respiratory Medicine Tokyo Dental College Ichikawa General Hospital Ichikawa Japan.ORCID https://orcid.org/0000-0002-8751-9600
Ho NamkoongDepartment of Infectious Diseases Keio University School of Medicine Shinjuku-ku Japan.
Eri IwamiDepartment of Respiratory Medicine Tokyo Dental College Ichikawa General Hospital Ichikawa Japan.
Akihiro TsutsumiDepartment of Respiratory Medicine Tokyo Dental College Ichikawa General Hospital Ichikawa Japan.
Takahiro NakajimaDepartment of Respiratory Medicine Tokyo Dental College Ichikawa General Hospital Ichikawa Japan.
Hajime ShinodaDepartment of Ophthalmology Keio University School of Medicine Shinjuku-ku Japan.
Yusaku KatadaDepartment of Ophthalmology Keio University School of Medicine Shinjuku-ku Japan.
Jiro IimuraDepartment of Otorhinolaryngology Tokyo Dental College Ichikawa General Hospital Ichikawa Japan.
Hisato SuzukiCenter for Medical Genetics Keio University School of Medicine Shinjuku-ku Japan.
Kenjiro KosakiCenter for Medical Genetics Keio University School of Medicine Shinjuku-ku Japan.
Takeshi TerashimaDepartment of Respiratory Medicine Tokyo Dental College Ichikawa General Hospital Ichikawa Japan.
Tokyo Dental College Ichikawa General Hospital · JPKeio University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bronchiectasis is a chronic respiratory condition characterized by irreversible bronchial dilation, often caused by infection or inflammation. It can be associated with primary ciliary dyskinesia (PCD), a hereditary disorder affecting cilia function in various organs and flagella. PCD's genetic heterogeneity leads to varying disease severity. PCD may be more prevalent in Asia, but its diagnosis is often delayed in Japan. This study reviewed a case of PCD and retinitis pigmentosa (RP) with the relevant literature. The patient had a persistent cough, sputum, and diffuse bronchiectasis. He was diagnosed with a combination of PCD and RP, with the presence of an X-linked retinitis pigmentosa GTPase regulator (

Indexed as

bronchiectasisinherited retinal dystrophyprimary ciliary dyskinesiaretinitis pigmentosaretinitis pigmentosa GTPase regulator

Identifiers

PMID37915370
PMCPMC10616737
OpenAlexW4388046692

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.