No mutation in the SLC2A2 (GLUT2) gene in a Turkish infant with Fanconi-Bickel syndrome

Ozer E., AKSU N., UCLAR E., ERDOGAN H., BAKILER A., TSUDA M., ...Daha Fazla

PEDIATRIC NEPHROLOGY, cilt.18, ss.397-398, 2003 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 18 Konu: 4
  • Basım Tarihi: 2003
  • Doi Numarası: 10.1007/s00467-003-1085-5
  • Sayfa Sayıları: ss.397-398


Fanconi-Bickel syndrome (FBS), or glycogen storage disease type XI, is a rare, well-defined clinical entity. Recently, this disease was elucidated to link mutations in the SLC2A2 gene in many ethnic groups, indicating that FBS is a single gene disease. We report here an 8-month-old Turkish girl who developed characteristic findings of FBS. However, no mutation was detected in the protein-coding region of the SLC2A2 gene. Therefore, we propose that further molecular analysis is needed to determine whether other genes are involved in FBS.