Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Adicionar filtros








Intervalo de ano
1.
Kidney Research and Clinical Practice ; : 287-291, 2018.
Artigo em Inglês | WPRIM | ID: wpr-717210

RESUMO

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.


Assuntos
Feminino , Humanos , Adenina Fosforribosiltransferase , Biópsia , Diagnóstico Precoce , Insuficiência Renal , Urolitíase
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA