Nephrotisches Syndrom im Kindesalter

Despite fulfilling the criteria for an orphan disease, idiopathic nephrotic syndrome in children is the most frequent glomerular disease in this age group. Nephrotic syndrome is defined by the detection of a high proteinuria (>1 g/m2 body surface area daily) and hypoalbuminemia (<2,5 g/dl). Ed...

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Bibliographic Details
Main Authors: Benz, Marcus R. (Author) , Ehren, Rasmus (Author) , Tönshoff, Burkhard (Author)
Format: Article (Journal)
Language:German
Published: 26 March 2019
In: Monatsschrift Kinderheilkunde
Year: 2019, Volume: 167, Issue: 6, Pages: 488-499
ISSN:1433-0474
DOI:10.1007/s00112-019-0677-5
Online Access:Verlag, Volltext: https://doi.org/10.1007/s00112-019-0677-5
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Author Notes:M.R. Benz, R. Ehren, B. Tönshoff, L.T. Weber
Description
Summary:Despite fulfilling the criteria for an orphan disease, idiopathic nephrotic syndrome in children is the most frequent glomerular disease in this age group. Nephrotic syndrome is defined by the detection of a high proteinuria (>1 g/m2 body surface area daily) and hypoalbuminemia (<2,5 g/dl). Edema is also mostly present, especially at the first manifestation. Nephrotic syndrome in children is a heterogeneous disease with respect to age of onset, etiology, histological alterations and response to a standard treatment of glucocorticoids. This diversity strongly influences both the differential diagnostic approach and the treatment. As the prognosis of steroid-sensitive nephrotic syndrome with respect to renal function is generally good, not only the efficacy of an immunosuppressive medication but also the side effect profiles of different immunosuppressive regimens should be kept in mind for treatment planning and optimization.
Item Description:Gesehen am 19.06.2019
Physical Description:Online Resource
ISSN:1433-0474
DOI:10.1007/s00112-019-0677-5