A genetic disorder with autosomal recessive inheritance, characterized by multiple CYSTS in both KIDNEYS and associated LIVER lesions. Serious manifestations are usually present at BIRTH with high PERINATAL MORTALITY.
Also Known As:
Polycystic Kidney Disease, Infantile, Type I; Polycystic Kidney, Autosomal Recessive; ARPKD; Polycystic Kidney Disease, Autosomal Recessive; Polycystic Kidney Disease, Infantile, Type 1; Polycystic Kidney and Hepatic Disease 1; Polycystic Kidney and Hepatic Disease 1 (Autosomal Recessive); Autosomal Recessive Polycystic Kidney Disease; Kidney, Polycystic, Autosomal Recessive