CORDIS Project
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This project aims to develop a new framework for understanding rare inherited kidney diseases by integrating phenotypic and genetic data. The goal is to identify biomarkers that can improve diagnosis and treatment, ultimately enhancing patient care.
Rare inherited kidney diseases (RIKDs) encompass over 150 different conditions.
They often lead to patients requiring renal replacement therapy being a major cause of end stage renal disease, severely compromising the patients’ quality of life and posing a high financial burden in healthcare.
They are characterised by a high degree of phenotypic heterogeneity and by the absence of biomarkers for disease diagnosis, prognosis and inadequate therapeutic management.
The main aim of the proposed work…
UNIVERSITY OF CYPRUS
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