Evidence map›Paper›PMID 41261870›Full record

ArticleJournal of clinical research in pediatric endocrinology2026

Single-Center Experience in Five Patients Diagnosed with Lipoid Congenital Adrenal Hyperplasia due to

Kürşat Çetin, Zeynep Donbaloğlu, Yasemin Funda Bahar, Ali Tırtar, Sezin Yakut Uzuner, Mesut Parlak, Hale Tuhan

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of clinical research in pediatric endocrinology, 2026. 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

7 authors.

Kürşat ÇetinAkdeniz University Hospital, Department of Pediatric Endocrinology, Antalya, TürkiyeORCID 0000-0002-9022-4010
Zeynep DonbaloğluAkdeniz University Hospital, Department of Pediatric Endocrinology, Antalya, TürkiyeORCID 0000-0003-0605-3229
Yasemin Funda BaharAkdeniz University Hospital, Department of Pediatric Endocrinology, Antalya, TürkiyeORCID 0000-0001-9022-5294
Ali TırtarAkdeniz University Hospital, Department of Pediatric Endocrinology, Antalya, TürkiyeORCID 0009-0001-9924-9775
Sezin Yakut UzunerAkdeniz University Hospital, Department of Medical Biology, Antalya, TürkiyeORCID 0000-0002-9540-5099
Mesut ParlakAkdeniz University Hospital, Department of Pediatric Endocrinology, Antalya, TürkiyeORCID 0000-0002-3550-1425
Hale TuhanAkdeniz University Hospital, Department of Pediatric Endocrinology, Antalya, TürkiyeORCID 0000-0002-7637-9630

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipoid congenital adrenal hyperplasia (LCAH) is the rarest and most severe form of congenital adrenal hyperplasia (CAH), characterized by impaired adrenal and gonadal steroidogenesis. This case series presents our clinical experience with five pediatric patients diagnosed with LCAH due to mutations in the

Indexed as

Adrenal Hyperplasia, CongenitalAdrenal InsufficiencyDisorder of Sex Development, 46,XYMutationPhosphoproteinsFemaleHumansInfantInfant, NewbornMaleRetrospective StudiesSteroidogenic Acute Regulatory ProteinPhosphoproteinsSteroidogenic Acute Regulatory Proteinadrenal insufficiencydisorders of sex developmentlipoid congenital adrenal hyperplasiasteroidogenic acute regulatory protein

Identifiers

PMID41261870
PMCPMC13325897

What OpenQuestion holds

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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.