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PMID: 17553488 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Correlation of the feline PKD1 genetic mutation with cases of PKD diagnosed by pathological examination.

Experimental and molecular pathology ·Vol. 83 ·No. 2 ·2007-10-00 ·页码 264-8

Helps C, Tasker S, Harley R

Abstract

Autosomal-dominant polycystic kidney disease (AD-PKD) is the most prevalent inherited genetic disease of cats, particularly affecting Persians. Using archived tissue samples from 44 cats a genotype was successfully obtained by real-time PCR for 43 cats. Twenty-five cats (18 Persians, 4 domestic longhair cats and 3 domestic shorthair (DSH) cats) were found to carry the AD-PKD mutation and all of these cats had macroscopic and/or microscopic evidence of renal cysts consistent with PKD. Eighteen cats were found to be wild-type. Twelve of these (all Persians) had no pathological evidence of PKD, but the remaining 6 cats had evidence of renal cystic lesions. On pathological review the cystic lesions in 4 (2 Persians and 2 DSH) of these 6 cats were considered not to be consistent with a primary diagnosis of PKD. Histological evidence of polycystic kidneys was, however, confirmed in the remaining 2 cats (1 DSH and 1 Bengal) and may indicate that other PKD-causing mutations exist in the feline population.

MeSH 主题词
Animals Cat Diseases/genetics Cats Genotype Polycystic Kidney, Autosomal Dominant/genetics,pathology,veterinary Polymerase Chain Reaction TRPP Cation Channels/metabolism
化学物质
TRPP Cation Channels polycystic kidney disease 1 protein
作者与单位
共 3 位作者,点击展开单位 / ORCID
Helps Chris
School of Clinical Veterinary Science, University of Bristol, Langford House, Langford, Bristol, BS40 5DU, UK. [email protected]
Tasker Séverine
Harley Ross
Article Info
Journal
Experimental and molecular pathology
Abbr.
Exp Mol Pathol
ISSN
0014-4800
Corresponding email
Published
2007-10-00
电子出版
2007-00-04
页码
264-8
Language
English
Country/Region
Netherlands
NLM ID
0370711
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