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Record W4410055528 · doi:10.1016/j.rare.2025.100092

Screening, diagnostic, and monitoring approaches of Bardet-Biedl Syndrome: A scoping review

2025· review· en· W4410055528 on OpenAlexaff
Letícia Nunes Campos, Ivo Valentin Rudzinski, Gabriela Oriana Pintos, Santino Curto, Santiago Miguel Maximowicz, Ayla Gerk, Israel Dávila Rivera, Federico Fernandez Zelcer, Carlos Stegmann, Carina F. Argüelles, Jorgelina Stegmann

Bibliographic record

VenueRare · 2025
Typereview
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicGenetic and Kidney Cyst Diseases
Canadian institutionsMcGill University Health Centre
FundersFondo Tecnológico Argentino
KeywordsBardet–Biedl syndromeMedicineBiologyGeneticsPhenotype

Abstract

fetched live from OpenAlex

Bardet-Biedl Syndrome (BBS) is a rare, autosomal recessive, multisystemic ciliopathy. Providing care for BBS presents challenges due to limited data. This scoping review aimed to characterize evidence for screening, diagnosing, and monitoring BBS. We searched ten databases for citations published in English and Spanish between January 2017 and October 2023. We selected human-based research that utilized methods to assess BBS, including experimental, quasi-experimental, observational studies, reviews, and guidelines. Screening and data extraction were performed by two independent reviewers, with a third reviewer involved to resolve disagreements. We employed descriptive statistical analyses and qualitative synthesis. We included 113 articles from 32 countries, mainly constituting case reports (n=45, 39.8%). Prenatal ultrasound was the most frequently reported screening method (n=15, 13.3%) for detecting early BBS indicators. Clinical manifestations were crucial in raising suspicion of BBS, with nearly all references adopting the diagnostic criteria by Forsythe and Beales. Central obesity (n=80, 70.8%), postaxial polydactyly (n=73, 64.6%), and retinal rod-cone dystrophy (n=56, 49.5%) were the most frequently documented manifestations. Genetic testing was also essential to diagnosing BBS, with techniques such as next-generation sequencing confirming up to 80% of cases. Articles reported variants in a total of 41 genes, including those encoding BBSome proteins, chaperones, and components of the IFT. Furthermore, we identified the most frequently assessed clinical features during patient follow-up. Notably, we observed that few articles reported complementary exams to evaluate BBS's clinical manifestations. Our results provide valuable insights for healthcare professionals, facilitating evidence-based, ongoing care for patients with BBS.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.015
metaresearch head score (Gemma)0.067
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Not applicable · Consensus signal: none
GenreCandidate signal: Review · Consensus signal: Review
Teacher disagreement score0.025
Threshold uncertainty score0.079

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0150.067
Meta-epidemiology (narrow)0.0020.001
Meta-epidemiology (broad)0.0050.005
Bibliometrics0.0250.018
Science and technology studies0.0010.001
Scholarly communication0.0040.004
Open science0.0020.002
Research integrity0.0030.001
Insufficient payload (model declined to judge)0.0040.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.051
GPT teacher head0.328
Teacher spread0.277 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designNot applicable
Domainnot available
GenreReview

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations3
Published2025
Admission routes1
Has abstractyes

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