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HNF1B nephropathy: for which congenital renal anomalies is genetic analysis advisable?

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Title: HNF1B nephropathy: for which congenital renal anomalies is genetic analysis advisable?
Authors: Flögelova H; Department of Pediatrics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Zdravotniku 248/7, 77900, Olomouc, Czech Republic. Hana.Flogelova@seznam.cz., Strasil R; Department of Pediatrics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Zdravotniku 248/7, 77900, Olomouc, Czech Republic.; Institute of Medical Genetics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Zdravotniku 248/7, 77900, Olomouc, Czech Republic.
Source: Pediatric nephrology (Berlin, Germany) [Pediatr Nephrol] 2026 Feb; Vol. 41 (2), pp. 263-265. Date of Electronic Publication: 2025 Jul 29.
Publication Type: Editorial
Journal Info: Publisher: Springer International Country of Publication: Germany NLM ID: 8708728 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-198X (Electronic) Linking ISSN: 0931041X NLM ISO Abbreviation: Pediatr Nephrol Subsets: MEDLINE; In Process
Database: MEDLINE Ultimate
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  Data: <searchLink fieldCode="AU" term="%22Flögelova+H%22">Flögelova H</searchLink>; Department of Pediatrics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Zdravotniku 248/7, 77900, Olomouc, Czech Republic. Hana.Flogelova@seznam.cz.<br /><searchLink fieldCode="AU" term="%22Strasil+R%22">Strasil R</searchLink>; Department of Pediatrics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Zdravotniku 248/7, 77900, Olomouc, Czech Republic.; Institute of Medical Genetics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Zdravotniku 248/7, 77900, Olomouc, Czech Republic.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Springer+International%22">Springer International </searchLink><i>Country of Publication: </i>Germany <i>NLM ID: </i>8708728 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1432-198X (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%220931041X%22">0931041X </searchLink><i>NLM ISO Abbreviation: </i>Pediatr Nephrol <i>Subsets: </i>MEDLINE; In Process
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        Value: 10.1007/s00467-025-06915-x
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      – Code: eng
        Text: English
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      – TitleFull: HNF1B nephropathy: for which congenital renal anomalies is genetic analysis advisable?
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              Text: 2026 Feb
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              Y: 2026
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