Ontology highlight
ABSTRACT:
SUBMITTER: Lopez de Heredia M
PROVIDER: S-EPMC8471778 | biostudies-literature | 2021 Sep
REPOSITORIES: biostudies-literature
López de Heredia Miguel M Muñoz Lourdes L Carru Ciriaco C Sotgia Salvatore S Zinellu Angelo A Serra Carmen C Llebaria Amadeu A Kato Yukio Y Nunes Virginia V
Antioxidants (Basel, Switzerland) 20210907 9
Cystinuria, a rare inherited aminoaciduria condition, is characterized by the hyperexcretion of cystine, ornithine, lysine, and arginine. Its main clinical manifestation is cystine stone formation in the urinary tract, being responsible for 1-2% total and 6-8% pediatric lithiasis. Cystinuria patients suffer from recurrent lithiasic episodes that might end in surgical interventions, progressive renal functional deterioration, and kidney loss. Cystinuria is monitored for the presence of urinary cy ...[more]