This website is intended for an Australian and New Zealand audience who are interested in acromegaly
This website is intended for an Australian and New Zealand audience who are interested in acromegaly

Who gets acromegaly?

Most people diagnosed with acromegaly are aged between 30 and 50 years of age, with men and women affected equally.

Very rarely (less than 1% of cases) acromegaly can be diagnosed in children and adolescents. Children and adolescents will, however, develop gigantism, whereas adults develop acromegaly.

Is acromegaly hereditary?

Acromegaly does sometimes run in families, but most of the time it’s not inherited.

Adenomas usually develop spontaneously because of a genetic change in a cell of the pituitary gland. This change causes uncontrolled growth of the affected cells, creating the tumour. Acromegaly does not occur because of any lifestyle choices or dietary reasons.

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Find out more about acromegaly

Diagnosing acromegaly

Find out how acromegaly is diagnosed and the tests that healthcare professionals may use to assess acromegaly symptoms

Diagnosis & Testing

Treating acromegaly

Read about acromegaly treatment options, including surgery, medications and radiotherapy, and the goals of therapy

Treating acromegaly

Acromegaly FAQs

Read and hear answers to some common questions that patients with acromegaly have asked

View FAQs
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Ipsen

Please always consult a healthcare professional if you require healthcare advice or if you have any specific concerns regarding your acromegaly, its treatment or side effects. The information provided here is not intended to replace professional advice. This website has been developed by Ipsen in collaboration with those living with acromegaly and the healthcare professionals who care for them. Ipsen would like to thank everyone for their valuable insights and stories. All names used on this website are not necessarily real names. Visit our website for more information about us, or to contact us directly. Website supported by Thrivase Pty Ltd.

SOM-AU-000711. Last reviewed: November 2023

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