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Polycystic kidney

Polycystic kidney is also known as Potter (I) syndrome, perlmann syndrome, congenital renal cystic tumor disease, cystic kidney, bilateral renal hypoplasia syndrome, benign multilocular cystic tumor of kidney and polycystic disease. Zhu Xianyi first reported in 1941 that this disease is not uncommon. There are two types of polycystic kidney, autosomal recessive (infantile) polycystic kidney, which occurs in infancy and is rare in clinic; Autosomal dominant (adult) polycystic kidney disease is often found in young and middle age, and can also occur at any age.

Symptoms

Multiple myeloma

Thalassemia

Simple purpura

Erythema multiforme

cholecystitis

Biliary ascariasis

Polycystic ovary syndrome

Hyperhidrosis

Single atrium

Simple pulmonary eosinophilia

Single ventricle

Cholesterol pneumonia

Escherichia coli pneumonia

Spinal vascular malformation type II and III

Choking

Multiple system organ failure

Typical preexcitation syndrome

Building disease syndrome

Multiple pulmonary infection

Amyloid cardiomyopathy

Common Health Issues

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