Evidence map›Paper›PMID 31213699›Full record

ReviewNature reviews. Endocrinology2019

Turner syndrome: mechanisms and management.

Claus H Gravholt, Mette H Viuff, Sara Brun, Kirstine Stochholm, Niels H Andersen

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Endocrinology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 173 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
173citing papers in PubMed, 5 pooled it
25.1field-weighted citation impact, top 1% 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

173 citing papers in PubMed, 5 syntheses or guidelines pooled it, 339 citations in OpenAlex.

  1. Turner Syndrome and the Thyroid Function-A Systematic and Critical Review.International journal of molecular sciences · 2024
    Pooled it
  2. X-linked genetic associations in sporadic thoracic aortic dissection.American journal of medical genetics. Part A · 2024
    Pooled it
  3. Pooled it
  4. Pooled it
  5. Guideline
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  7. Review
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  16. A Rare Coexistence of Turner Syndrome and Mycosis Fungoides: A Case ReportJournal of clinical research in pediatric endocrinology · 2026
    Article
  17. Article
  18. Article
  19. Article
  20. Article

113 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 1 country.

Claus H GravholtDepartment of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark. ch.gravholt@dadlnet.dk.ORCID http://orcid.org/0000-0001-5924-1720
Mette H ViuffDepartment of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark.ORCID http://orcid.org/0000-0001-6574-4893
Sara BrunDepartment of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark.ORCID http://orcid.org/0000-0002-3708-2949
Kirstine StochholmDepartment of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark.
Niels H AndersenDepartment of Cardiology, Aalborg University Hospital, Aalborg, Denmark.ORCID http://orcid.org/0000-0002-5394-3016
Aarhus University Hospital · DKAalborg University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Turner syndrome is a rare condition in women that is associated with either complete or partial loss of one X chromosome, often in mosaic karyotypes. Turner syndrome is associated with short stature, delayed puberty, ovarian dysgenesis, hypergonadotropic hypogonadism, infertility, congenital malformations of the heart, endocrine disorders such as type 1 and type 2 diabetes mellitus, osteoporosis and autoimmune disorders. Morbidity and mortality are increased in women with Turner syndrome compared with the general population and the involvement of multiple organs through all stages of life necessitates a multidisciplinary approach to care. Despite an often conspicuous phenotype, the diagnostic delay can be substantial and the average age at diagnosis is around 15 years of age. However, numerous important clinical advances have been achieved, covering all specialty fields involved in the care of girls and women with Turner syndrome. Here, we present an updated Review of Turner syndrome, covering advances in genetic and genomic mechanisms of disease, associated disorders and multidisciplinary approaches to patient management, including growth hormone therapy and hormone replacement therapy.

Indexed as

Disease ManagementFemaleHeart Defects, CongenitalHormone Replacement TherapyHuman Growth HormoneHumansTurner SyndromeHuman Growth Hormone

Identifiers

PMID31213699
OpenAlexW2950018554

What Socratic 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 Socratic graph.