Great chats - marking the NSMC take-over of NephJC. Visual Abstract by Sinead, NephJC hosting from Diana and Sinead, moments curated by Michelle Starr (with a bonus moment from Maryam Khosravi)
Nephrocystin: the Visual Abstract
Here is the visual abstract from NSMC intern Sinead Stoneman.
Also new this week: we turn over the reigns of #NephJC even for the hosting duties
Full visual abstract at this link.
We also have a Spanish version of the Visual Abstract, courtesy Pablo Garcia:
Nephrocystin: More Notable than we thought?
To most Nephrologists, Nephronophthisis (NPH) is considered to be a rare autosomal recessive paediatric disease. However, this article by Snoek et al challenges that belief, by examining the prevalence of mutations that cause NPH, in adults with end stage renal disease (ESRD). Read our NephJC summary below and come along to our Twitter Journal Club discussion to find out whether you might consider a diagnosis of NPH, next time you see that patient carrying a label of ‘ESRD, cause unknown’.