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Fanconi-Bickel syndrome in three Turkish patients with different homozygous mutations
Inci Nur Saltik-Temizel1, Turgay Coşkun, Aysel Yüce
1Section of Gastroenterology, Hepatology and Nutrition, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.
The Turkish Journal of Pediatrics
|August 2, 2005
Abstract:
Three Turkish patients with Fanconi-Bickel syndrome are presented. Prominent clinical findings of patients included hepatomegaly, growth retardation, hypoglycemia, characteristic tubular nephropathy, and rickets. Each patient had a different homozygous mutation of glucose transporter 2 (GLUT2) gene.
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