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Updated: Aug 6, 2026

Spectral Karyotyping to Study Chromosome Abnormalities in Humans and Mice with Polycystic Kidney Disease
Published on: February 3, 2012
Autosomal recessive polycystic kidney disease (ARPKD)
Klaus Zerres1, Sabine Rudnik-Schöneborn, Jan Senderek
1Institute for Human Genetics, Aachen University of Technology, Aachen, Germany. kzerres@ukaachen.de
Abstract:
Autosomal recessive polycystic kidney disease (ARPKD) is an important hereditary early childhood nephropathy. However, the clinical ARPKD spectrum is much more variable than is generally presumed. Presentation of ARPKD at a later age and survival into adulthood is well known. Diagnostic criteria, clinical course, differential diagnoses, genetics and molecular biology will be discussed along with the advantages and limitations of mutation detection in clinical practice.
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