Universität zu Köln

Liebau, Max Christoph ORCID: 0000-0003-0494-9080 (2021). Early clinical management of autosomal recessive polycystic kidney disease. Pediatr. Nephrol., 36 (11). S. 3561 - 3571. NEW YORK: SPRINGER. ISSN 1432-198X

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Abstract

Autosomal recessive polycystic kidney disease (ARPKD) is a rare but highly relevant disorder in pediatric nephrology. This genetic disease is mainly caused by variants in the PKHD1 gene and is characterized by fibrocystic hepatorenal phenotypes with major clinical variability. ARPKD frequently presents perinatally, and the management of perinatal and early disease symptoms may be challenging. This review discusses aspects of early manifestations in ARPKD and its clincial management with a special focus on kidney disease.

Item Type:	Journal Article
Creators:	Creators Email ORCID ORCID Put Code Liebau, Max Christoph UNSPECIFIED orcid.org/0000-0003-0494-9080 UNSPECIFIED
URN:	urn:nbn:de:hbz:38-563900
DOI:	10.1007/s00467-021-04970-8
Journal or Publication Title:	Pediatr. Nephrol.
Volume:	36
Number:	11
Page Range:	S. 3561 - 3571
Date:	2021
Publisher:	SPRINGER
Place of Publication:	NEW YORK
ISSN:	1432-198X
Language:	English
Faculty:	Unspecified
Divisions:	Unspecified
Subjects:	no entry
Uncontrolled Keywords:	Keywords Language Pediatrics; Urology & Nephrology Multiple languages
URI:	http://kups.ub.uni-koeln.de/id/eprint/56390