Polycystic kidney disease in Persian cats closely resembles the autosomal p
olycystic kidney disease in human beings. Both diseases are inherited as au
tosomal dominant traits. They are characterized by the development and enla
rgment of cysts in the renal cortex and medulla resulting in progressive re
nomegaly. Finally, both diseases usually are accompanied by renal failure l
ate in life. The marked clinical and morphological similarities of APKD in
Persian cats and the human disease, as well as the autosomal dominant inher
itance pattern, suggest that the feline condition is a potential model for
the study of APKD in humans.