Evidence map›Paper›PMID 36242011›Full record

ArticleJournal of medical case reports2022

Syrian females with congenital adrenal hyperplasia: a case series.

Nada Dehneh, Rami Jarjour, Sahar Idelbi, Assad Alibrahem, Sahar Al Fahoum

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

Article in Journal of medical case reports, 2022. 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
0.2field-weighted citation impact, top 51% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  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

5 authors at 3 institutions in 1 country.

Nada DehnehDept. of Biochemistry and Microbiology, Faculty of Pharmacy, Damascus University, Damascus, Syria. nada1971dehneh@gmail.com.
Rami JarjourClinical Genetics Unit, Atomic Energy Commission of Syria (AECS), Damascus, Syria.
Sahar IdelbiUnit of Pediatric Endocrinology and Metabolism, Children's Hospital, Damascus, Syria.
Assad AlibrahemUnit of Pediatric Endocrinology and Metabolism, Children's Hospital, Damascus, Syria.
Sahar Al FahoumDept. of Biochemistry and Microbiology, Faculty of Pharmacy, Damascus University, Damascus, Syria.
Damascus Hospital · SYDamascus University · SYArab International University · SY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOne of the most common types of congenital adrenal hyperplasia is an autosomal recessive disorder with 21-hydroxylase deficiency. The classical form, defined by cortisol insufficiency, is accompanied by prenatal androgen excess causing variable masculinization degrees of external genitalia in babies with a 46, XX karyotype. CASES PRESENTATION: These five case reports highlight the management of Syrian females aged between 0 and 32 years with congenital adrenal hyperplasia. Two of the patients have been raised as males, while two had reconstructive surgery and one had hormonal therapy. Becoming mother was achieved by two patients

conclusionThe integrated treatment of females with classical congenital adrenal hyperplasia CAH, which includes appropriate surgical procedures and controlled hormonal therapy, gives these females the opportunity to live as they are, and perhaps as mothers in the future.

Indexed as

Adrenal Hyperplasia, CongenitalAdolescentAdultAndrogensChildChild, PreschoolFemaleHumansHydrocortisoneInfantInfant, NewbornMalePregnancySyriaYoung AdultAndrogensHydrocortisoneCase reportCongenital adrenal hyperplasiaSyria

Identifiers

PMID36242011
PMCPMC9569117
OpenAlexW4306248868

What OpenQuestion holds

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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.