Mapping the locus of autosomal dominant polycystic kidney disease: Diagnostic application

S. T. Reeders, G. G. Germino, G. A J Gillespie

Research output: Contribution to journalArticlepeer-review

Abstract

Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common autosomal dominant disorders affecting humans. The recent identification of a number of restriction fragment length polymorphisms linked to ADPKD now offers a method for diagnosis in families that are large enough for linkage and phase of linkage to be established. Initial studies of >50 families with the disease localized all disease-producing mutations to the short arm of chromosome 16. Recently, however, families have been identified in which linkage to 16p markers cannot be detected. Such genetic heterogeneity of linkage limits the value of diagnostic methods based on linkage analysis and focuses attention on the need for direct diagnosis of disease-producing mutations. This in turn requires the isolation, cloning, and characterization of ADPKD genes. A refined map of the region around the PKD1 gene, the ADPKD gene localized on chromosome 16p, is presented.

Original languageEnglish (US)
JournalClinical Chemistry
Volume35
Issue number7 SUPPL.
StatePublished - 1989
Externally publishedYes

ASJC Scopus subject areas

  • Clinical Biochemistry

Fingerprint Dive into the research topics of 'Mapping the locus of autosomal dominant polycystic kidney disease: Diagnostic application'. Together they form a unique fingerprint.

Cite this