Evidence map›Paper›PMID 38784773›Full record

ArticleOxford medical case reports2024

A rare case of steroid 11 beta-hydroxylase deficiency in a child revealed by acute pulmonary edema.

Zohair El Haddar, Aziza El Ouali, Ayad Ghanam, Noufissa Benajiba, Maria Rkain, Abdeladim Babakhouya

Abstract readCase Reports
In one paragraph

Article in Oxford medical case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Zohair El HaddarDepartment of Pediatrics, Mohammed VI University Hospital, Oujda, Morocco.ORCID https://orcid.org/0000-0003-0419-7691
Aziza El OualiDepartment of Pediatrics, Mohammed VI University Hospital, Oujda, Morocco.
Ayad GhanamDepartment of Pediatrics, Mohammed VI University Hospital, Oujda, Morocco.
Noufissa BenajibaDepartment of Pediatrics, Mohammed VI University Hospital, Oujda, Morocco.
Maria RkainDepartment of Pediatrics, Mohammed VI University Hospital, Oujda, Morocco.
Abdeladim BabakhouyaDepartment of Pediatrics, Mohammed VI University Hospital, Oujda, Morocco.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report the case of a 5-year-old boy diagnosed with congenital adrenal hyperplasia due to 11-hydroxylase deficiency, revealed by disorders of sex development (DSD) and acute pulmonary edema due to severe hypertension. We considered the diagnosis based on biological and radiological examinations. The sociocultural background and the delayed diagnosis had a significant impact on the therapeutic decisions. All babies should be screened for 11 beta-hydroxylase deficiency, there should be specialized and interdisciplinary medical centers, and early detection is essential to avoiding serious complications of this disease.

Identifiers

PMID38784773
PMCPMC11110861

What OpenQuestion holds

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Registered trials

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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.