Clinical Notes
Congenital glucose–galactose malabsorption diagnosed from macrohematuria in an infant
Ryoko Yoshimura,
Ryoko Yoshimura
Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan
Search for more papers by this author Tohru Fujii,
Corresponding Author
Tohru Fujii
Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan
Correspondence: Tohru Fujii, MD PhD, Department of Pediatrics, Juntendo University Faculty of Medicine, 2-1-1, Hongo, Bunkyo-ku, Tokyo 113-8421, Japan. Email:
[email protected]Search for more papers by this author Amane Endo,
Amane Endo
Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan
Search for more papers by this author Takahiro Kudo,
Takahiro Kudo
Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan
Search for more papers by this author Toshiaki Shimizu,
Toshiaki Shimizu
Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan
Search for more papers by this author
Ryoko Yoshimura,
Ryoko Yoshimura
Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan
Search for more papers by this author Tohru Fujii,
Corresponding Author
Tohru Fujii
Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan
Correspondence: Tohru Fujii, MD PhD, Department of Pediatrics, Juntendo University Faculty of Medicine, 2-1-1, Hongo, Bunkyo-ku, Tokyo 113-8421, Japan. Email:
[email protected]Search for more papers by this author Amane Endo,
Amane Endo
Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan
Search for more papers by this author Takahiro Kudo,
Takahiro Kudo
Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan
Search for more papers by this author Toshiaki Shimizu,
Toshiaki Shimizu
Department of Pediatrics, Juntendo University Faculty of Medicine, Tokyo, Japan
Search for more papers by this author
First published: 23 December 2016
No abstract is available for this article.
References
- 1Vallaeys L, Van Biervliet S, De Bruyn G et al. Congenital glucose-galactose malabsorption: a novel deletion within the SLC5A1 gene. Eur. J. Pediatr. 2013; 172: 409–11.
- 2Saarela T, Similä S, Koivisto M. Hypercalcemia and nephrocalcinosis in patients with congenital lactase deficiency. J. Pediatr. 1995; 127: 920–3.
- 3El-Naggar W, Balfe JW, Barbar M, Taha D. Nephrocalcinosis in glucose-galactose malabsorption, association with renal tubular acidosis. Pediatr. Nephrol. 2005; 20: 1336–9.
- 4Soylu OB, Ecevit CO, Altinoz S et al. Nephrocalcinosis in glucose-galactose malabsorption: nephrocalcinosis and proximal tubular dysfunction in a young infant with a novel mutation of SGLT1. Eur. J. Pediatr. 2008; 167: 1395–8.
- 5Abdullah AM, el-Mouzan MI, el Shiekh OK, al Mazyad A. Congenital glucose-galactose malabsorption in Arab children. J. Pediatr. Gastroenterol. Nutr. 1996; 23: 561–4.
