Adenine phosphoribosyltransferase (APRT) deficiency: a new genetic mutation with early recurrent renal stone disease in kidney transplantation

Adenine phosphoribosyltransferase (APRT) deficiency, a rare inborn error inherited as an autosomic recessive trait, presents with 2,8-dihydroxyadenine (2,8-DHA) crystal nephropathy. We describe clinical, biochemical and molecular findings in a renal transplant recipient with renal failure, 2,8-DHA s...

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Detalles Bibliográficos
Autores principales: Micheli, Vanna, Massarino, Fabio, Jacomelli, Gabriella, Bertelli, Matteo, Corradi, Maria Rita, Guerrini, Andrea, Cucchiara, Antonino, Ravetti, Jean Louis, Negretti, Laura, Cannella, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2010
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421695/
https://www.ncbi.nlm.nih.gov/pubmed/25984046
http://dx.doi.org/10.1093/ndtplus/sfq096

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421695/
https://www.ncbi.nlm.nih.gov/pubmed/25984046
http://dx.doi.org/10.1093/ndtplus/sfq096

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