Evidence map›Paper›PMID 26898950›Full record

ReviewThe British journal of radiology2016

Sclerosing bone dysplasias: genetic, clinical and radiology update of hereditary and non-hereditary disorders.

Cedric Boulet, Hardi Madani, Leon Lenchik, Filip Vanhoenacker, Deepak S Amalnath, Johan de Mey, Michel De Maeseneer

Open access · greenAbstract readReview
In one paragraph

Review in The British journal of radiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.5field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 57 citations in OpenAlex.

  1. Melorheostotic Bone Lesions Caused by Somatic Mutations in MAP2K1 Have Deteriorated Microarchitecture and Periosteal Reaction.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2019
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  11. Bone and growth: basic principles behind rare disorders.Wiener medizinische Wochenschrift (1946) · 2021
    Article
  12. Review
  13. The dripping candle wax sign of melorheostosis.SAGE open medical case reports · 2020
    Article
  14. Review
  15. Article
  16. Article
  17. Osteopoikilosis in the Mandible.Contemporary clinical dentistry
    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 4 institutions in 4 countries.

Cedric Boulet1 Department of Radiology, Universitair Ziekenhuis Brussel, Brussel, Belgium.
Hardi Madani2 Department of Radiology, Royal Free Hospital, London, UK.
Leon Lenchik3 Department of Radiology, Wake Forest University, Winston Salem, NC, USA.
Filip Vanhoenacker4 Department of Radiology, Universitair Ziekenhuis Anwerpen, Antwerpen, Belgium.
Deepak S Amalnath5 Department of Medicine, Indira Gandhi Medical College and Research Institute, Pondicherry, India.
Johan de Mey1 Department of Radiology, Universitair Ziekenhuis Brussel, Brussel, Belgium.
Michel De Maeseneer1 Department of Radiology, Universitair Ziekenhuis Brussel, Brussel, Belgium.
Universitair Ziekenhuis Brussel · BEIndira Gandhi Medical College and Research Institute · INThe Royal Free Hospital · GBWake Forest University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a wide variety of hereditary and non-hereditary bone dysplasias, many with unique radiographic findings. Hereditary bony dysplasias include osteopoikilosis, osteopathia striata, osteopetrosis, progressive diaphyseal dysplasia, hereditary multiple diaphyseal sclerosis and pyknodysostosis. Non-hereditary dysplasias include melorheostosis, intramedullary osteosclerosis and overlap syndromes. Although many of these dysplasias are uncommon, radiologists should be familiar with their genetic, clinical and imaging findings to allow for differentiation from acquired causes of bony sclerosis. We present an overview of hereditary and non-hereditary bony dysplasias with focus on the pathogenesis, clinical and radiographic findings of each disorder.

Indexed as

Bone Diseases, DevelopmentalDiagnosis, DifferentialEvidence-Based MedicineGenetic Predisposition to DiseaseHumansOsteosclerosis

Identifiers

PMID26898950
PMCPMC5258139
OpenAlexW2280350038

What OpenQuestion holds

Textmetadata
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.