Understanding Acromegaly

Acromegaly is a rare condition that affects three to four out of every million people per year.

As a condition, acromegaly was first identified in 1886. It affects the growth of bone and skeletal muscles, the way the body uses proteins, fats, carbohydrates, and the growth of skin cells. It is known as an "acquired" condition because it is generally not hereditary, it develops sometime after birth.

Acromegaly is a condition that progresses slowly, so slowly that it often is not diagnosed until many years after it starts. Without treatment, acromegaly can affect your long-term health. Fortunately, acromegaly can be treated successfully to protect your health and quality of life. However, to receive the full benefits of therapy, you should receive treatment as soon as possible.

Caused by too much growth hormone

Acromegaly occurs when levels of growth hormone and insulin-like growth factor are too high. Learn more about the causes of acromegaly.

Symptoms

Typically, acromegaly causes abnormal growth of bones in the body, usually those in the hands and the face. Read about the symptoms of acromegaly.

Diagnosis

Healthcare professionals diagnose acromegaly based on symptoms they can see and on tests to show them what they can't see. Read about the diagnosis of acromegaly.