Saudi Journal of Kidney Diseases and Transplantation

ARTICLES
Year
: 2003  |  Volume : 14  |  Issue : 3  |  Page : 351--357

Cystinosis and Cystinuria: Differences in Outcome


Karl S Roth1, James CM Chan2 
1 Departments of Pediatrics, Creighton University, Omaha, NE, USA
2 Barbara Bush Children's Hospital, Maine Medical Center, Portland, ME and University of Vermont, Burlington, VT, USA

Correspondence Address:
Karl S Roth
Department of Pediatrics, Creighton University, Omaha, NE
USA

Cystinosis and cystinuria, both recessive genetic disorders, are fundamentally different in their pathophysiologic mechanisms. Cystinosis is a disease of cystine storage in which the kidney is the initial, but not the sole target organ. Cystinuria is a disease of renal tubular cystine transport in which excessive loss of this insoluble amino acid causes precipitation at physiologic urine pH and concentration. The former disorder uniformly results in the need for renal allograft despite recent advances in medical therapy. Cystinuria has a variable severity of expression and may be amenable to long-term medical treatment in some patients. Others may have frequent stone recurrence and infection and progress to chronic renal failure in the long term. It is the purpose of this review to provide the reader with an understanding of the respective diseases and the reasons for the differences in their prognoses and long-term outcomes.


How to cite this article:
Roth KS, Chan JC. Cystinosis and Cystinuria: Differences in Outcome.Saudi J Kidney Dis Transpl 2003;14:351-357


How to cite this URL:
Roth KS, Chan JC. Cystinosis and Cystinuria: Differences in Outcome. Saudi J Kidney Dis Transpl [serial online] 2003 [cited 2021 Apr 23 ];14:351-357
Available from: https://www.sjkdt.org/article.asp?issn=1319-2442;year=2003;volume=14;issue=3;spage=351;epage=357;aulast=Roth;type=0