Identification of genetic causes for sporadic steroid-resistant nephrotic syndrome in adults

Monogenic forms of Steroid-Resistant Nephrotic Syndrome (SRNS) have been widely characterized, but genetic screening paradigms preferentially address congenital, infantile onset, and familial cases. Our aim was to characterize the distribution of disease-causing gene mutations in adults with sporadi...

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Veröffentlicht in:	Kidney international 2018-11, Vol.94 (5), p.1013-1022
Hauptverfasser:	Gribouval, Olivier, Boyer, Olivia, Hummel, Aurélie, Dantal, Jacques, Martinez, Frank, Sberro-Soussan, Rebecca, Etienne, Isabelle, Chauveau, Dominique, Delahousse, Michel, Lionet, Arnaud, Allard, Julien, Pouteil Noble, Claire, Tête, Marie-Josèphe, Heidet, Laurence, Antignac, Corinne, Servais, Aude
Format:	Artikel
Sprache:	eng
Schlagworte:	Adaptor Proteins, Signal Transducing - genetics Adolescent Adult Aged Aged, 80 and over Alport syndrome Apolipoprotein L1 - genetics Autoantigens - genetics collagen Collagen Type IV - genetics Cytoskeletal Proteins - genetics Drug Resistance Female focal segmental glomerulosclerosis genetic Glucocorticoids - therapeutic use Humans Kidney - pathology Male Middle Aged Mutation Nephrotic Syndrome - drug therapy Nephrotic Syndrome - genetics steroid-resistant nephrotic syndrome Young Adult
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