Evidence map›Paper›PMID 28808977›Full record

ReviewCurrent osteoporosis reports2017

Skeletal Dysplasias: What Every Bone Health Clinician Needs to Know.

Sarah M Nikkel

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current osteoporosis reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 14 citations in OpenAlex.

  1. Not all the bowlegs is rickets! (a case report).The Pan African medical journal · 2022
    Article
  2. Article
  3. Revisiting the Population Genetics of Human Height.Journal of the Endocrine Society · 2020
    Article
  4. Review
  5. Changes in skeletal dysplasia nosology.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    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

1 author at 1 institution in 1 country.

Sarah M NikkelProvinical Medical Genetics Program, BC Women's Hospital and Health Centre, University of British Columbia, 4500 Oak Street, Vancouver, BC, V6H 3N1, Canada. sarah.nikkel@cw.bc.ca.
University of British Columbia · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewThis review highlights how skeletal dysplasias are diagnosed and how our understanding of some of these conditions has now translated to treatment options. RECENT

findingsThe use of multigene panels, using next-generation sequence technology, has improved our ability to quickly identify the genetic etiology, which can impact management. There are successes with the use of growth hormone in individuals with SHOX deficiencies, asfotase alfa in hypophosphatasia, and some promising data for c-type natriuretic peptide for those with achondroplasia. One needs to consider that a patient with short stature has a skeletal dysplasia as options for management may be available.

Indexed as

AchondroplasiaAlkaline PhosphataseBone Diseases, DevelopmentalEnzyme Replacement TherapyGenetic TestingHigh-Throughput Nucleotide SequencingHuman Growth HormoneHumansHypophosphatasiaImmunoglobulin GNatriuretic AgentsNatriuretic Peptide, C-TypeOsteochondrodysplasiasOsteogenesis ImperfectaRadiographyRecombinant Fusion ProteinsAlkaline Phosphataseasfotase alfaHuman Growth HormoneImmunoglobulin GNatriuretic AgentsNatriuretic Peptide, C-TypeRecombinant Fusion ProteinsRecombinant ProteinsShort Stature Homeobox ProteinC-type natriuretic peptideEnzyme replacement therapyGene panelsRadiographsSkeletal dysplasias

Identifiers

PMID28808977
OpenAlexW2747488432

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.