Evidence map›Paper›PMID 33750447›Full record

ArticleItalian journal of pediatrics2021

Definition and prevalence of familial short stature.

Veronica Grigoletto, Alessandro Agostino Occhipinti, Maria Chiara Pellegrin, Fabio Sirchia, Egidio Barbi, Gianluca Tornese

Open access · goldAbstract read
In one paragraph

Article in Italian journal of pediatrics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 30% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
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  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Monogenic causes of familial short stature.Frontiers in endocrinology · 2024
    Review
  10. 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

6 authors at 2 institutions in 1 country.

Veronica GrigolettoUniversity of Trieste, Trieste, Italy.ORCID https://orcid.org/0000-0001-6247-5739
Alessandro Agostino OcchipintiUniversity of Trieste, Trieste, Italy.ORCID https://orcid.org/0000-0002-8084-3328
Maria Chiara PellegrinInstitute for Maternal and Child Health - IRCCS "Burlo Garofolo" - Trieste, Via dell'Istria 65/1, 34137, Trieste, Italy.ORCID https://orcid.org/0000-0002-0801-3645
Fabio SirchiaInstitute for Maternal and Child Health - IRCCS "Burlo Garofolo" - Trieste, Via dell'Istria 65/1, 34137, Trieste, Italy.ORCID https://orcid.org/0000-0002-4598-2023
Egidio BarbiUniversity of Trieste, Trieste, Italy.ORCID https://orcid.org/0000-0002-6343-846X
Gianluca TorneseInstitute for Maternal and Child Health - IRCCS "Burlo Garofolo" - Trieste, Via dell'Istria 65/1, 34137, Trieste, Italy. gianluca.tornese@burlo.trieste.it.ORCID http://orcid.org/0000-0002-4395-3915
IRCCS Materno Infantile Burlo Garofolo · ITUniversity of Trieste · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo verify the prevalence of novel definitions of familial short stature on a cross-sectional cohort of children referred for short stature when their height and that of both parents were measured.

methodsWe consecutively enrolled 65 individuals referred for short stature when both parents were present. We defined "target height-related short stature" (TH-SS) when child's height is ≤ - 2 SDS and included in the range of target height; suspected "autosomal dominant short stature" (AD-SS) when child height and at least one parent height are ≤ - 2 SDS; "constitutional familial short stature" (C-FSS) when a child with TH-SS does not have any parents with height ≤ - 2 SDS.

resultsOf 65 children referred for SS, 48 individuals had a height ≤ - 2 SDS. Based on the parents' measured heights, 24 children had TH-SS, 16 subjects AD-SS, and 12 individuals C-FSS. If we had considered only the parents' reported height, 3 of 24 children with TH-SS, 9 of 16 with AD-SS, and 10 of 12 with C-FSS would have been lost.

conclusionWe suggest novel definitions to adequately detect and approach the cases of FSS since C-FSS (25%) might not need any specific investigation, while on the contrary, AD-SS (33%) should undergo genetic evaluation. Moreover, this study underlines that adequate measurement and consideration of children's and parents' heights (individually and together) are crucial in the clinical evaluation of every child with short stature.

Indexed as

Body HeightParentsAdolescentChildChild, PreschoolCohort StudiesCross-Sectional StudiesDwarfismFemaleGrowth DisordersHumansMaleFamilial short statureGeneticsMeasuredReportedTarget height

Identifiers

PMID33750447
PMCPMC7941953
OpenAlexW3111887045

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.