Hepatocyte Nuclear Factor 1 Beta Mutation-associated Newborn Onset of Glomerulocystic Kidney Disease: A Case Presentation

Mutations in hepatocyte nuclear factor-1 beta ( ) are the most commonly identified genetic cause of renal malformations. Heterozygous mutations are associated with renal cysts and diabetes syndrome. Various renal developmental abnormalities and maturity-onset diabetes of the young could be the prese...

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Veröffentlicht in:	Medeniyet medical journal 2021-12, Vol.36 (4), p.352-355
Hauptverfasser:	Goknar, Nilufer, Ekici Avci, Melda, Uckardes, Diana, Kelesoglu, Emre, Tekkus Ermis, Kubra, Candan, Cengiz
Format:	Artikel
Sprache:	eng
Schlagworte:	Case Report
Online-Zugang:	Volltext
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