[Skip to Content]
[Skip to Content Landing]
Article
May 1955

RARE CASE OF POLYCYSTIC DISEASE OF THE KIDNEYS

Author Affiliations

Fresno, Calif.
Resident physician (Dr. Liang).; Department of Pathology, Valley Children's Hospital and Guidance Clinic (Dr. Bocian).

AMA Am J Dis Child. 1955;89(5):615-617. doi:10.1001/archpedi.1955.02050110729021
Abstract

POLYCYSTIC disease of the kidney is relatively uncommon in children. It is generally believed that the cysts are due to a failure of union between the secretory and collecting portions of the kidney unit. Polycystic disease of the kidney is mostly bilateral, but unilateral involvement has been reported. Bell has expressed the opinion that polycystic kidneys are inherited as a Mendelian dominant. Cairns and others list the defects with which it is most frequently associated, such as harelip, spina bifida, atresia ani, and defects of kdneys, ureters, and sex organs. Rall and Odel have found associated congenital anomalies encountered in polycystic disease of the kidneys, as polycystic liver, polycystic pancreas, polycystic spleen, cardiac defects, defects of nervous system, and defects of musculoskeletal system.

Potter classifies the polycystic kidneys found in the fetus or young infant into two groups: (1) those in which the amount of renal connective tissue is normal

First Page Preview View Large
First page PDF preview
First page PDF preview
×