Evidence map›Paper›PMID 27384690›Full record

ArticlePediatric nephrology (Berlin, Germany)2017

Rare case of nephrocalcinosis in a 14-year-old girl: Questions.

Omar Bjanid, Piotr Adamczyk, Małgorzata Stojewska, Dagmara Roszkowska-Bjanid, Magdalena Paszyna-Grześkowiak, Agnieszka Jędzura, Joanna Oświęcimska, Katarzyna Ziora, Aurelia Morawiec-Knysak, Maria Szczepańska

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

Article in Pediatric nephrology (Berlin, Germany), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. Abnormal teeth and renal calcifications: Answers.Pediatric nephrology (Berlin, Germany) · 2023
    Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Omar BjanidDepartment of Pediatric Nephrology with Dialysis Division for Children, Public Clinical Hospital No. 1, ul. 3 Maja 13/15, 41-800, Zabrze, Poland.
Piotr AdamczykChair and Clinical Department of Pediatrics, School of Medicine with the Division of Dentistry in Zabrze, Medical University of Silesia in Katowice, ul. 3 Maja 13/15, 41-800, Zabrze, Poland.
Małgorzata StojewskaChair and Clinical Department of Pediatrics, School of Medicine with the Division of Dentistry in Zabrze, Medical University of Silesia in Katowice, ul. 3 Maja 13/15, 41-800, Zabrze, Poland.
Dagmara Roszkowska-BjanidDepartment of Pediatric Nephrology with Dialysis Division for Children, Public Clinical Hospital No. 1, ul. 3 Maja 13/15, 41-800, Zabrze, Poland.
Magdalena Paszyna-GrześkowiakDepartment of Pediatric Nephrology with Dialysis Division for Children, Public Clinical Hospital No. 1, ul. 3 Maja 13/15, 41-800, Zabrze, Poland.
Agnieszka JędzuraDepartment of Pediatric Nephrology with Dialysis Division for Children, Public Clinical Hospital No. 1, ul. 3 Maja 13/15, 41-800, Zabrze, Poland.
Joanna OświęcimskaChair and Clinical Department of Pediatrics, School of Medicine with the Division of Dentistry in Zabrze, Medical University of Silesia in Katowice, ul. 3 Maja 13/15, 41-800, Zabrze, Poland.
Katarzyna ZioraChair and Clinical Department of Pediatrics, School of Medicine with the Division of Dentistry in Zabrze, Medical University of Silesia in Katowice, ul. 3 Maja 13/15, 41-800, Zabrze, Poland.
Aurelia Morawiec-KnysakDepartment of Pediatric Nephrology with Dialysis Division for Children, Public Clinical Hospital No. 1, ul. 3 Maja 13/15, 41-800, Zabrze, Poland.
Maria SzczepańskaChair and Clinical Department of Pediatrics, School of Medicine with the Division of Dentistry in Zabrze, Medical University of Silesia in Katowice, ul. 3 Maja 13/15, 41-800, Zabrze, Poland. szczep57@poczta.onet.pl.
Medical University of Silesia · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A 14-year-old Caucasian girl with a history of primary hypoparathyroidism and unstable calcium and phosphorus levels and on ongoing treatment was admitted to the Department of Pediatric Nephrology because of the onset of nephrocalcinosis and difficulties achieving normocalcemia. Coexistence of hypoparathyroidism, oral candidiasis, dental enamel hypoplasia, and subclinical Hashimoto's disease was strongly suggestive for autoimmune polyglandular syndrome (APS) type I. One of the clinical implications of this diagnosis is the high probability of future occurrence of adrenal insufficiency and hence the importance of maintaining a high level of suspicion in case of the onset of symptoms like weakness, fainting, hypotonia, or hyperkaliemia. Addison's disease would, in fact, be quite challenging for the future management of this patient.This clinical quiz highlighted the importance of careful evaluation of all multiorgan symptoms occurring in a patient to prevent further complications.

Indexed as

Addison DiseaseAdolescentAutoimmune DiseasesBasal GangliaFemaleHumansHypoparathyroidismKidney Function TestsNephrocalcinosisPolyendocrinopathies, AutoimmuneTomography, X-Ray ComputedUltrasonographyAutoimmune polyendocrine syndrome type 1ChildrenHypoparathyroidismNephrocalcinosis

Identifiers

PMID27384690
PMCPMC5334399
OpenAlexW2471164926

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.