Evidence map›Paper›PMID 33407701›Full record

ReviewOrphanet journal of rare diseases2021

Bone fragility in patients affected by congenital diseases non skeletal in origin.

L Masi, S Ferrari, M K Javaid, S Papapoulos, D D Pierroz, M L Brandi, IOF Skeletal Rare Diseases Working Group

Open access · goldAbstract readReview
In one paragraph

Review in Orphanet journal of rare diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Applications of DNA Hydrogels in Osteoporotic Bone Defects.Journal of functional biomaterials · 2026
    Review
  3. Review
  4. Review
  5. Article
  6. 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

7 authors at 5 institutions in 4 countries.

L MasiMetabolic Bone Diseases Unit, University Hospital of Florence, AOU-Careggi, Florence, Italy.
S FerrariDivision of Bone Diseases, Faculty of Medicine, Geneva University Hospital, Geneva, Switzerland.
M K JavaidOxford NIHR Musculoskeletal Biomedical Research Unit, University of Oxford, Oxford, UK.
S PapapoulosCenter for Bone Quality, Leiden University Medical Center, Leiden, The Netherlands.
D D PierrozInternational Osteoporosis Foundation (IOF), Rue Juste-Olivier 9, 1260, Nyon, Switzerland.
M L BrandiFondazione Italiana Ricerca sulle Malattie dell'Osso, Florence, Italy. marialuisa.brandi@unifi.it.ORCID 0000-0002-8741-0592
IOF Skeletal Rare Diseases Working Group
Azienda Ospedaliero-Universitaria Careggi · ITFondazione Studio Marangoni · ITLeiden University Medical Center · NLUniversity Hospital of Geneva · CHUniversity of Oxford · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBone tissue represents a large systemic compartment of the human body, with an active metabolism, that controls mineral deposition and removal, and where several factors may play a role. For these reasons, several non-skeletal diseases may influence bone metabolism. It is of a crucial importance to classify these disorders in order to facilitate diagnosis and clinical management. This article reports a taxonomic classification of non-skeletal rare congenital disorders, which have an impact on bone metabolism

methodsThe International Osteoporosis Foundation (IOF) Skeletal Rare Diseases Working Group (SRD-WG), comprised of basic and clinical scientists, has decided to review the taxonomy of non-skeletal rare disorders that may alter bone physiology.

resultsThe taxonomy of non-skeletal rare congenital disorders which impact bone comprises a total of 6 groups of disorders that may influence the activity of bone cells or the characteristics of bone matrix.

conclusionsThis paper provides the first comprehensive taxonomy of non-skeletal rare congenital disorders with impact on bone physiology.

Indexed as

Musculoskeletal DiseasesOsteoporosisBone and BonesHumansRare DiseasesResearch ReportBone metabolismGenetic bone diseasesMetabolic bone diseasesNon-skeletal rare congenital disordersTaxonomy

Identifiers

PMID33407701
PMCPMC7789665
OpenAlexW3120694894

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.