Pierson syndrome with numerous dilated tubules masquerading as autosomal recessive polycystic kidney disease: a case report.

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Title: Pierson syndrome with numerous dilated tubules masquerading as autosomal recessive polycystic kidney disease: a case report.
Authors: Yamamura-Miyazaki N; Department of Pediatric Nephrology and Metabolism, Osaka Women's and Children's Hospital, 840 Murodo-cho, 594-1101, Izumi, Osaka, Japan. yamamur@wch.opho.jp., Michigami T; Department of Pediatric Nephrology and Metabolism, Osaka Women's and Children's Hospital, 840 Murodo-cho, 594-1101, Izumi, Osaka, Japan.; Department of Bone and Mineral Research, Research Institute, Osaka Women's and Children's Hospital, Osaka, Japan., Okamoto N; Department of Medical Genetics, Osaka Women's and Children's Hospital, Osaka, Japan., Iida T; Department of Genome Medicine, National Center for Child Health and Development, Tokyo, Japan., Yanagi K; Department of Genome Medicine, National Center for Child Health and Development, Tokyo, Japan., Kaname T; Department of Genome Medicine, National Center for Child Health and Development, Tokyo, Japan., Fukuda S; Department of Fetal Medicine, Osaka Women's and Children's Hospital, Osaka, Japan., Baba M; Department of Pediatric Nephrology and Metabolism, Osaka Women's and Children's Hospital, 840 Murodo-cho, 594-1101, Izumi, Osaka, Japan., Fujiwara K; Department of Pediatric Nephrology and Metabolism, Osaka Women's and Children's Hospital, 840 Murodo-cho, 594-1101, Izumi, Osaka, Japan., Kubota T; Department of Pediatric Nephrology and Metabolism, Osaka Women's and Children's Hospital, 840 Murodo-cho, 594-1101, Izumi, Osaka, Japan.
Source: CEN case reports [CEN Case Rep] 2026 Apr 18; Vol. 15 (3). Date of Electronic Publication: 2026 Apr 18.
Publication Type: Journal Article; Case Reports
Journal Info: Publisher: Springer Japan Country of Publication: Japan NLM ID: 101636244 Publication Model: Electronic Cited Medium: Internet ISSN: 2192-4449 (Electronic) Linking ISSN: 21924449 NLM ISO Abbreviation: CEN Case Rep Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:2192-4449
DOI:10.1007/s13730-026-01105-6