Universität zu Köln

Weigert, Alexander, Beck, Bodo B. and Hoppe, Bernd (2018). Genetic kidney stone disesases. Med. Genet., 30 (4). S. 438 - 448. HEIDELBERG: SPRINGER HEIDELBERG. ISSN 1863-5490

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Abstract

The incidence and prevalence of stone diseases have significantly increased over the last few years. It is crucial to correctly diagnose the underlying condition to initiate proper treatment as early as possible and thus prevent devastating consequences such as end-stage renal failure. In up to 75% of pediatric patients genetic or anatomical causes can be identified. The various underlying conditions are presented here according to each lithogenic risk factor and, if available, the appropriate therapeutic approaches are elucidated.

Item Type:	Journal Article
Creators:	Creators Email ORCID ORCID Put Code Weigert, Alexander UNSPECIFIED UNSPECIFIED UNSPECIFIED Beck, Bodo B. UNSPECIFIED UNSPECIFIED UNSPECIFIED Hoppe, Bernd UNSPECIFIED UNSPECIFIED UNSPECIFIED
URN:	urn:nbn:de:hbz:38-162859
DOI:	10.1007/s11825-018-0227-x
Journal or Publication Title:	Med. Genet.
Volume:	30
Number:	4
Page Range:	S. 438 - 448
Date:	2018
Publisher:	SPRINGER HEIDELBERG
Place of Publication:	HEIDELBERG
ISSN:	1863-5490
Language:	German
Faculty:	Unspecified
Divisions:	Unspecified
Subjects:	no entry
Uncontrolled Keywords:	Keywords Language PRIMARY HYPEROXALURIA TYPE-1; RISK-FACTORS; UROLITHIASIS; NEPHROCALCINOSIS; TRANSPLANTATION; MUTATIONS; NEPHROLITHIASIS; CYSTINURIA; DIAGNOSIS; CHILDREN Multiple languages Genetics & Heredity Multiple languages
Refereed:	Yes
URI:	http://kups.ub.uni-koeln.de/id/eprint/16285