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Kidney Research and Clinical Practice ; : 287-291, 2018.
Artículo en Inglés | WPRIM | ID: wpr-717210

RESUMEN

Adenine phosphoribosyltransferase enzyme deficiency is a rare, autosomal recessive disorder. It is a disease limited to the renal system and usually presents with urolithiasis. Herein, we report a young female with dihydroxyadenine (DHA) crystal-induced nephropathy presenting with rapidly progressive renal failure. DHA crystals can be easily diagnosed by their pathognomic color and shape in urine and biopsy specimens. A high index of clinical suspicion helps in the early diagnosis of this potentially treatable renal disease.


Asunto(s)
Femenino , Humanos , Adenina Fosforribosiltransferasa , Biopsia , Diagnóstico Precoz , Insuficiencia Renal , Urolitiasis
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