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adult polycystic kidney

Adult polycystic kidney is an autosomal dominant genetic disease. Almost all of them are bilateral. Adult polycystic kidney usually has no symptoms before the age of 40, and multiple cysts of the same shape can be seen in the liver, spleen and pancreas. The volume of polycystic kidney is larger than that of normal kidney, and its surface is covered with cysts of different sizes.

Symptoms

Globus pallidus nigra erythronuclear pigmented degeneration

Postpartum psychosis

Postpartum depression

Tremor syndrome

Intestinal gram negative bacilli meningitis

Dementia syndrome

CM1 ganglioside storage disease

Persistent vegetative state

tic and convulsion

Tourette syndrome

Hemorrhagic cerebral infarction

Post traumatic stress disorder

Pure autonomic nerve failure

Cluster headache

Status epilepticus

Pituitary dwarfism

Pituitary apoplexy

Postpartum thyroiditis

Adult total hypophysis

Adult female breast hypertrophy

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