Evidence map›Paper›PMID 42779582›Full record

ArticleChildhood kidney diseases2026

Very-early-onset autosomal dominant polycystic kidney disease coexisting with congenital adrenal hyperplasia in a newborn: a case report.

Chang Kim, Hwa Young Kim, Young Hwa Jung, Chang Won Choi, Jaehyun Kim, Ji Hyun Kim

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

Article in Childhood kidney diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

6 authors.

Chang KimDepartment of Pediatrics, Seoul National University Children's Hospital, Seoul, Republic of Korea.ORCID 0000-0002-6867-2335
Hwa Young KimDepartment of Pediatrics, Seoul National University College of Medicine, Seoul, Republic of Korea.ORCID 0000-0003-3238-5315
Young Hwa JungDepartment of Pediatrics, Seoul National University College of Medicine, Seoul, Republic of Korea.ORCID 0000-0002-4159-586X
Chang Won ChoiDepartment of Pediatrics, Seoul National University College of Medicine, Seoul, Republic of Korea.ORCID 0000-0003-1911-0253
Jaehyun KimDepartment of Pediatrics, Seoul National University College of Medicine, Seoul, Republic of Korea.ORCID 0000-0002-0203-7443
Ji Hyun KimDepartment of Pediatrics, Seoul National University College of Medicine, Seoul, Republic of Korea.ORCID 0000-0001-8477-0157

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This case report describes a newborn diagnosed with very-early-onset autosomal dominant polycystic kidney disease (VEO-ADPKD) and congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency. The patient presented with prenatally detected kidney cysts and exhibited clinical and laboratory features consistent with salt-wasting, including markedly elevated 17-hydroxyprogesterone levels, requiring treatment with hydrocortisone, fludrocortisone, and sodium chloride. Genetic analysis revealed a

Indexed as

Adrenal hyperplasia, congenitalCase reportsInfant, newbornPolycystic kidney, autosomal dominant

Identifiers

PMID42779582
PMCPMC13587212

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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.