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Dihydroxyadenine crystal-induced nephropathy presenting with rapidly progressive renal failure
Kidney Research and Clinical Practice ; : 287-291, 2018.
Article in English | WPRIM | ID: wpr-717210
ABSTRACT
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.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Biopsy / Adenine Phosphoribosyltransferase / Early Diagnosis / Renal Insufficiency / Urolithiasis Type of study: Diagnostic study / Screening study Limits: Female / Humans Language: English Journal: Kidney Research and Clinical Practice Year: 2018 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Biopsy / Adenine Phosphoribosyltransferase / Early Diagnosis / Renal Insufficiency / Urolithiasis Type of study: Diagnostic study / Screening study Limits: Female / Humans Language: English Journal: Kidney Research and Clinical Practice Year: 2018 Type: Article