Evidence map›Paper›PMID 36011254›Full record

ArticleGenes2022

McCune-Albright Syndrome in Infant with Growth Hormone Excess.

Katarina Brzica, Marko Simunovic, Matea Ivancic, Darija Tudor, Ivna Skrabic, Veselin Skrabic

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Genes, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. 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.

Katarina BrzicaDepartment of Pediatrics, University Hospital of Split, Spinciceva 1, 21000 Split, Croatia.ORCID 0000-0002-9644-4516
Marko SimunovicDepartment of Pediatrics, University Hospital of Split, Spinciceva 1, 21000 Split, Croatia.
Matea IvancicDepartment of Pediatrics, Sibenik General Hospital, Stjepana Radica 83, 22000 Sibenik, Croatia.
Darija TudorDepartment of Pediatrics, University Hospital of Split, Spinciceva 1, 21000 Split, Croatia.
Ivna SkrabicDepartment of Pediatrics, University Hospital of Split, Spinciceva 1, 21000 Split, Croatia.
Veselin SkrabicDepartment of Pediatrics, University Hospital of Split, Spinciceva 1, 21000 Split, Croatia.
University of Split · HRŠibenik University of Applied Sciences · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMcCune-Albright is a rare syndrome, caused by mutation of the CASE REPORT: We present the case of a patient who is, to the best of our knowledge and after extensive review of literature, the youngest McCune-Albright syndrome patient with growth hormone excess, diagnosed at 8.9 months of age. An extensive diagnostic procedure was done upon the diagnosis. Hormonal assessment was performed and all hormone levels were within reference range, and an additional oral glucose suppression that noted the presence of growth hormone excess. Magnetic resonance imaging of the pituitary gland did not detect a tumor process. The genetic analysis of the

conclusionThis case report emphasizes the lack of available data on treatment of growth hormone excess and follow-up in pediatric population and the need for further research.

Indexed as

AcromegalyFibrous Dysplasia, PolyostoticCafe-au-Lait SpotsChildHumansSyndromecafe au lait maculesgrowth hormone excessMcCune-Albright syndromeoctreotide

Identifiers

PMID36011254
PMCPMC9407244
OpenAlexW4288066938

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.