Evidence map›Paper›PMID 41504382›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2026

Diagnosis, treatment, and management recommendations for cleidocranial dysplasia: A modified Delphi panel.

Julie Hoover-Fong, Cheryl Anderson-Cermin, Frank Artinian, Stella Chaushu, Mike Harrison, Suzanne M Jan de Beur, Klane K White, Kelly Wosnik, Nnenna Ene, M Elizabeth Wegman and 2 more

Abstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Julie Hoover-FongDepartment of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, United States.ORCID 0000-0002-1242-5626
Cheryl Anderson-CerminUniversity of Minnesota School of Dentistry, Minneapolis, MN 55455, United States.
Frank ArtinianDepartments of Newborn Medicine and Pediatric Hospital Medicine, Akron Children's Hospital, Akron, OH 44308, United States.ORCID 0000-0001-7430-4769
Stella ChaushuHadassah Medical Center, Faculty of Dental Medicine, Hebrew University of Jerusalem, Jerusalem 91120, Israel.ORCID 0000-0001-9571-8338
Mike HarrisonDepartment of Paediatric Dentistry, Guy's and St Thomas' NHS Foundation Trust, London SE1 7EH, United Kingdom.
Suzanne M Jan de BeurDivision of Endocrinology and Metabolism, Department of Medicine, University of Virginia School of Medicine, Charlottesville, VA 22908, United States.ORCID 0000-0002-9386-7732
Klane K WhiteDepartment of Orthopedics, University of Colorado School of Medicine, Aurora, CO 80045, United States.
Kelly WosnikBristol Health, Orem, UT 84057, United States.
Nnenna EneCostello Medical, Boston, MA 02108, United States.
M Elizabeth WegmanCostello Medical, Boston, MA 02108, United States.
Marielle BrownCostello Medical, Boston, MA 02108, United States.
Ilana M ZinnDepartment of Plastic and Reconstructive Surgery, Johns Hopkins University School of Medicine, Baltimore, MD 21287, United States.

Funding

CCD Smiles Foundation
6 · The paper itself

Abstract

Cleidocranial dysplasia is a rare genetic condition negatively impacting skeletal development. Clinical guidelines for patients, their family members, and clinicians on the diagnosis, treatment, and management of this disease are lacking. The aim of this study was to align expert opinion on standard of care (SoC) medical recommendations for patients with cleidocranial dysplasia, primarily for adults and children (≥2 yrs of age). A modified Delphi panel comprised of a 3-round survey was used to determine consensus among a multidisciplinary team of 13 experts with experience treating patients with cleidocranial dysplasia. Statements for Round 1 were generated from a targeted literature review and received input from a steering committee of 2 experts within the panel. Expert discussion held after Round 2 helped refine statements for Round 3; the steering committee also reviewed statements before dissemination in each round. The consensus threshold was pre-defined as ≥70% agreement or disagreement for Likert-scale statements or ≥70% of experts selecting the same response for a multiple-choice option. For statements wherein consensus was measured, 79% (n/N = 26/33), 91% (n/N = 21/23), and 100% (n/N = 12/12) of statements reached consensus, respectively, in Round 1, Round 2, and Round 3. Overall, consensus was reached on 37 SoC recommendations for patients with cleidocranial dysplasia: 9 regarding diagnosis, 24 regarding treatment and management, consisting of 7 dental/orthodontic and 17 other medical (non-dental/orthodontic), and 4 regarding care providers. The expert consensus reached in this panel informs the first comprehensive best practice guidelines for patients, their family members, and healthcare providers to diagnose, treat, and manage the dental/orthodontic and other medical complications of cleidocranial dysplasia.

Indexed as

Cleidocranial DysplasiaDelphi TechniqueAdultChildConsensusFemaleHumanscleidocranial dysplasiadentalmodified Delphi panelRUNX2skeletalstandard of care recommendations

Identifiers

PMID41504382
PMCPMC13525201

What OpenQuestion holds

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Registered trials

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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.