American Journal of Kidney Diseases
Volume 53, Issue 3 , Pages 546-549 , March 2009

Neonatal Acidosis With Nephrocalcinosis: A Clinical Approach

Received 23 April 2008 ,Accepted 17 September 2008.

References 

  1. Rake JP, Visser G, Labrune P, Leonard JV, Ullrich K, Smit JPA. Guidelines for management of glycogen storage disease type I (European study on glycogen storage disorder type 1). Eur J Pediatr. 2002;161:S112–S119
  2. Ronnefarth G, Misselwitz J. Arbeitgemeinschaft fur Padiatrische Nephrologie: Nephrocalcinosis in children: A retrospective review. Pediatr Nephrol. 2000;14:1016–1021
  3. Mantan M, Bagga A, Virdi VS, Menon S, Hari P. Etiology of nephrocalcinosis in northern Indian children. Pediatr Nephrol. 2007;22:829–833
  4. Chen Y. Glycogen storage diseases. In:  Behrman RE,  Kliegman RM,  Jenson HB editor. Textbook of Pediatrics. (ed 17). Philadelphia, PA: Saunders; 2004;p. 469–475
  5. Chen YT, Coleman RA, Scheinman JI, Kolbeck PC, Sidbury JB. Renal disease in type I glycogen storage disorder. N Engl J Med. 1988;318:7–11
  6. Chen YT. Type I glycogen storage disorder: Kidney involvement, pathogenesis and its treatment. Pediatr Nephrol. 1991;5:71–76
  7. Weinstein DA, Somers MJG, Wolfsdorf JI. Decreased urinary citrate excretion in type Ia glycogen storage disease. J Pediatr. 2001;138:378–382
  8. Guven AG, Koyum M, Artan R, Dursum O, Baysal YE, Akman S. Severe lactic acidosis and nephrolithiasis in an infant—Etiology?. Pediatr Nephrol. 2006;21:761–762
  9. Lin CC, Tsai JD, Lin SP, Lee HC. Renal sonographic findings of type 1 glycogen storage disease in infancy and early childhood. Pediatr Radiol. 2005;35:786–791
  10. Chen YT, Cornblath M, Sidbury JB. Cornstarch therapy in glycogen storage disease. N Engl J Med. 1984;310:171–175
  11. Chen YT, Scheinman JI, Park HK, Coleman RA, Roe CR. Amelioration of proximal renal tubular dysfunction in type I glycogen storage disease with dietary therapy. N Engl J Med. 1990;323:590–593

 Originally published online as doi:10.1053/j.ajkd.2008.09.009 on November 13, 2008.

PII: S0272-6386(08)01360-7

doi: 10.1053/j.ajkd.2008.09.009

American Journal of Kidney Diseases
Volume 53, Issue 3 , Pages 546-549 , March 2009