Evidence map›Paper›PMID 40686918›Full record

ArticleCase reports in pediatrics2025

Severe Hypocalcemia Dependent on Fluconazole in a Newborn With Barakat Syndrome.

Dorota Roztoczyńska, Anna Wędrychowicz, Magdalena Ossowska, Aleksandra Furtak, Paulina Miśkiewicz-Stanek, Ewelina Preizner-Rzucidło, Joanna Kwinta-Rybicka, Mateusz Jagła, Jerzy B Starzyk

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PubMed Full text at PMC Publisher
In one paragraph

Article in Case reports in pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Dorota RoztoczyńskaDepartment of Pediatric and Adolescent Endocrinology, Department of Pediatrics, Institute of Pediatrics, Collegium Medicum, Jagiellonian University, Krakow, Poland.ORCID https://orcid.org/0000-0003-1754-0137
Anna WędrychowiczDepartment of Pediatric and Adolescent Endocrinology, Department of Pediatrics, Institute of Pediatrics, Collegium Medicum, Jagiellonian University, Krakow, Poland.ORCID https://orcid.org/0000-0003-0864-6810
Magdalena OssowskaDepartment of Pediatric and Adolescent Endocrinology, Department of Pediatrics, Institute of Pediatrics, Collegium Medicum, Jagiellonian University, Krakow, Poland.ORCID https://orcid.org/0000-0002-8122-5265
Aleksandra FurtakDepartment of Pediatric and Adolescent Endocrinology, Department of Pediatrics, Institute of Pediatrics, Collegium Medicum, Jagiellonian University, Krakow, Poland.ORCID https://orcid.org/0000-0001-6527-940X
Paulina Miśkiewicz-StanekDepartment of Pediatric and Adolescent Endocrinology, Department of Pediatrics, Institute of Pediatrics, Collegium Medicum, Jagiellonian University, Krakow, Poland.ORCID https://orcid.org/0009-0009-3498-9770
Ewelina Preizner-RzucidłoDepartment of Genetics, Institute of Pediatrics, Collegium Medicum, Jagiellonian University, Krakow, Poland.ORCID https://orcid.org/0009-0005-2904-4300
Joanna Kwinta-RybickaDepartment of Pediatric Nephrology and Hypertension, Institute of Pediatrics, Collegium Medicum, Jagiellonian University, Krakow, Poland.ORCID https://orcid.org/0000-0002-3706-584X
Mateusz JagłaDepartment of Neonatology and Intensive Care, Department of Pediatrics, Institute of Pediatrics, Collegium Medicum, Jagiellonian University, Krakow, Poland.ORCID https://orcid.org/0000-0002-7030-3934
Jerzy B StarzykDepartment of Pediatric and Adolescent Endocrinology, Department of Pediatrics, Institute of Pediatrics, Collegium Medicum, Jagiellonian University, Krakow, Poland.ORCID https://orcid.org/0000-0002-4086-6525

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present a case of a newborn with Barakat syndrome, characterized by congenital hypoparathyroidism, severe hypocalcemia, recurrent urinary tract infections (UTIs), and congenital candidiasis, which is an atypical feature for this syndrome. The patient, born at term, exhibited dysmorphia, hearing loss, and renal dysfunction. Genetic testing revealed a novel, de novo

Indexed as

hearing losshypoparathyroidismkidney diseasesneonatal hypocalcemia

Identifiers

PMID40686918
PMCPMC12271702

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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.