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Dihydroxyadenine crystal-induced nephropathy presenting with rapidly progressive renal failure
Article em En | WPRIM | ID: wpr-717210
Biblioteca responsável: WPRO
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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Texto completo: 1 Índice: WPRIM Assunto principal: Biópsia / Adenina Fosforribosiltransferase / Diagnóstico Precoce / Insuficiência Renal / Urolitíase Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Female / Humans Idioma: En Revista: Kidney Research and Clinical Practice Ano de publicação: 2018 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Assunto principal: Biópsia / Adenina Fosforribosiltransferase / Diagnóstico Precoce / Insuficiência Renal / Urolitíase Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Female / Humans Idioma: En Revista: Kidney Research and Clinical Practice Ano de publicação: 2018 Tipo de documento: Article