A case of Fanconi syndrome accompanied by crystal depositions in tubular cells in a patient with multiple myeloma

• Main Authors: Do Hee Kim (Author), A Young Lim (Author), Hye Bin Gwag (Author), Ji Hyeon Lee (Author), Ki Sun Jung (Author), Keol Lee (Author), Wooseong Huh (Author), Dae Joong Kim (Author), Yoon-Goo Kim (Author), Ha Young Oh (Author), Kihyun Kim (Author), Gee-Young Kwon (Author), Jung Eun Lee (Author)
• Format: Book
• Published: The Korean Society of Nephrology, 2014-06-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Fanconi syndrome (FS) is a rare condition that is characterized by defects in the proximal tubular function. A 48-year-old woman was admitted for evaluation of proteinuria. The patient showed normal anion gap acidosis, normoglycemic glycosuria, hypophosphatemia, and hypouricemia. Thus, her condition...