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Updated: Apr 15, 2026

Isolation, Characterization, And High Throughput Extracellular Flux Analysis of Mouse Primary Renal Tubular Epithelial Cells
Published on: June 20, 2018
Two patients with HNF4A-related congenital hyperinsulinism and renal tubular dysfunction: A clinical variation which
Chikahiko Numakura1, Yukiko Hashimoto2, Takashi Daitsu1
1Department of Pediatrics, Yamagata University School of Medicine, Yamagata, Japan.
Abstract:
The HNF4A p.R76W mutation causes congenital hyperinsulinism with Fanconi syndrome. Here, we report two cases who also presented with increased urinary calcium excretion and one had a transient hepatic dysfunction with hepatomegaly. Clinical variations including transient liver dysfunction is a likely mutation-specific clinical characteristic.
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