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Abstract
Kidney dysplasia is one of the most frequent causes of chronic kidney failure in children. While dysplasia is a histological diagnosis, the term “kidney dysplasia” is frequently used in daily clinical life without histopathological confirmation. Clinical parameters of kidney dysplasia have not been clearly defined, leading to imprecise communication amongst healthcare professional and with patients. This lack of consensus hampers precise disease understanding and the development of specific therapies. Based on a structured literature search, we here suggest a common basis for clinical, imaging, genetic, pathological, and basic science aspects of non-obstructive kidney dysplasia associated with functional kidney impairment.
We propose to accept hallmark sonographic findings as surrogate parameters defining a clinical diagnosis of dysplastic kidneys. We suggest differentiated clinical follow-up plans for children with kidney dysplasia and summarize established monogenic causes for non-obstructive kidney dysplasia. Finally, we point out and discuss research gaps in the field.
We propose to accept hallmark sonographic findings as surrogate parameters defining a clinical diagnosis of dysplastic kidneys. We suggest differentiated clinical follow-up plans for children with kidney dysplasia and summarize established monogenic causes for non-obstructive kidney dysplasia. Finally, we point out and discuss research gaps in the field.
Original language | English |
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Journal | Nephrology Dialysis Transplantation |
Publication status | Accepted/In press - 15 Jun 2022 |
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Dive into the research topics of 'Definition, diagnosis, and clinical management of nonobstructive kidney dysplasia: A consensus statement by the ERKNet working group on Kidney Malformations'. Together they form a unique fingerprint.Projects
- 1 Finished
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Preclinical Gene Therapy for Genetic urinary Bladder Disease.
Woolf, A. (PI) & Roberts, N. (CoI)
1/01/20 → 28/02/22
Project: Research