Evidence map›Paper›PMID 36348931›Full record

ArticleCureus2022

Bardet-Biedl Syndrome: A Rare Case From Ophthalmology Perspective.

Mustafa Alhamoud, Ghadah Alnosair, Hassan Alhashim

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Cureus, 2022. 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
0.7field-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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

3 authors at 3 institutions in 2 countries.

Mustafa AlhamoudOphthalmology, King Fahd Hospital of the University, Dammam, SAU.
Ghadah AlnosairPediatric Ophthalmology and Strabismus, Dammam Medical Complex, Dammam, SAU.
Hassan AlhashimOphthalmology, Imam Abdulrahman Bin Faisal University, Dammam, SAU.
Dammam Central Hospital · SAImam Abdulrahman Bin Faisal University · SAStrabismus Research Foundation · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bardet-Biedl syndrome (BBS) is a rare multisystem disease, with autosomal recessive inheritance and genetic heterogeneity characterized by post-axial polydactyl, cone-rods dystrophy, and central obesity. BBS involves many organs in the body with variable complications and the life span of affected individuals. Clinical confirmation of the disorder can be done using a revised criterion that consists of primary or major features and secondary or minor features. Primary features of BBS include hypogonadism, polydactyly, obesity, retinitis pigmentosa, and learning disability. While ataxia, poor coordination, brachydactyly, diabetes mellitus, speech abnormalities, liver fibrosis, hearing loss, spasticity, and cardiovascular anomaly constitute the secondary features. In this study, we report a case of a five-year-old Saudi girl who presented with language delay, delay in milestones, progressive weight gain, excised polydactyly, and retinitis pigmentosa. An integrated medicine approach would substantially improve the quality of life of the affected individuals and their families by enhancing both physical and mental health.

Indexed as

bardet-biedl syndromeconsanguineous marriagelaurence-moon-bardet-biedl syndromepolydactylyrelatives’ marriageretinitis pigmentosa

Identifiers

PMID36348931
PMCPMC9632917
OpenAlexW4301373904

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.