| Literature DB >> 27181776 |
Craig B Langman1, Bruce A Barshop2, Georges Deschênes3, Francesco Emma4, Paul Goodyer5, Graham Lipkin6, Julian P Midgley7, Chris Ottolenghi8, Aude Servais9, Neveen A Soliman10, Jess G Thoene11, Elena N Levtchenko12.
Abstract
Nephropathic cystinosis is an autosomal recessive metabolic, lifelong disease characterized by lysosomal cystine accumulation throughout the body that commonly presents in infancy with a renal Fanconi syndrome and, if untreated, leads to end-stage kidney disease (ESKD) in the later childhood years. The molecular basis is due to mutations in CTNS, the gene encoding for the lysosomal cystine-proton cotransporter, cystinosin. During adolescence and adulthood, extrarenal manifestations of cystinosis develop and require multidisciplinary care. Despite substantial improvement in prognosis due to cystine-depleting therapy with cysteamine, no cure of the disease is currently available. Kidney Disease: Improving Global Outcomes (KDIGO) convened a Controversies Conference on cystinosis to review the state-of-the-art knowledge and to address areas of controversies in pathophysiology, diagnostics, monitoring, and treatment in different age groups. More importantly, promising areas of investigation that may lead to optimal outcomes for patients afflicted with this lifelong, systemic disease were discussed with a research agenda proposed for the future.Entities:
Keywords: biomarker; cell signaling; chronic kidney disease; cystinosin; end-stage kidney disease; rare kidney diseases
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Year: 2016 PMID: 27181776 DOI: 10.1016/j.kint.2016.01.033
Source DB: PubMed Journal: Kidney Int ISSN: 0085-2538 Impact factor: 10.612