Ontology highlight
ABSTRACT: Objectives
This study was aimed at detecting feline autosomal dominant polycystic kidney disease in a population of Persian and Persian-related breeds by a molecular method in Iran.Methods
Buccal swab samples were collected from 47 cats and examined with a touchdown PCR method. Additionally, partial sequencing was performed in two cats with bilateral renal cysts.Results
Twenty-two cats (46.8%) were diagnosed as heterozygous for this mutation. Sequence analysis of two cats showed C to A point mutation in the PKD1 gene, as in previous studies.Conclusions and relevance
Prevalence of this disease is high in Iran, highlighting the need for molecular screening tests before including cats in breeding programmes.
SUBMITTER: Moazezi Ghavihelm A
PROVIDER: S-EPMC8808032 | biostudies-literature | 2022 Jan-Jun
REPOSITORIES: biostudies-literature
Moazezi Ghavihelm Ali A Jamshidi Shahram S Ashrafi Tamai Iraj I Zangisheh Mahsa M
JFMS open reports 20220130 1
<h4>Objectives</h4>This study was aimed at detecting feline autosomal dominant polycystic kidney disease in a population of Persian and Persian-related breeds by a molecular method in Iran.<h4>Methods</h4>Buccal swab samples were collected from 47 cats and examined with a touchdown PCR method. Additionally, partial sequencing was performed in two cats with bilateral renal cysts.<h4>Results</h4>Twenty-two cats (46.8%) were diagnosed as heterozygous for this mutation. Sequence analysis of two cats ...[more]