Polycystic kidney disease was first described in adult male and female long-haired, Persian-type cats in the late 1960’s. In 1996, the disorder was shown to be inherited as an autosomal dominant trait in a family of Persian cats. Both male and female cats were affected. In affected × unaffected crosses, 42% of offspring were affected and 58% were unaffected. In affected × affected crosses, 73% ...

M.D. Second Edition. Pp. xii., 434. Bristol: John Wright & Co. 1896. These lectures, first issued as two separate works, are now revised and published in a single volume with additions, including a special section on stone in the kidney, hydronephrosis, pyelitis, and hsemoglobinuria. Dr. Saundby's views are so clear, and his theories so well expressed, that we heartily welcome the reappearance ...

Recent progress in molecular genetics has strongly influenced nephrology. Gene mutations have been identified which cause various monogenic hereditary renal diseases including Alport syndrome, autosomal dominant polycystic kidney disease, and tubular transporter disorders. The data obtained will be useful not only to develop new methods of diagnosis and treatment of such particular diseases but...

Patients with chronic renal disease (CRD) represent an important segment of Tunisian population, and mostly because of the high risk of cardiovascular disease (CVD) associated with renal insufficiency, detection and treatment of chronic renal disease is now a public health priority (Abderrahim E et al., 2001, Ben Maïz H et al., 2006, Counil E et al., 2008). The increased incidence of CVD is lik...