Acromegaly

Not yet reviewed

This information is AI generated and has not yet been reviewed by a specialist physician. AI can make mistakes.

Disease overview

Disorder characterized by excessive growth hormone (GH) production

Common symptoms

Wide variety of symptoms and physical findingscharacterisitic facial prominencegradual enlargement of hands and feet [ ].

When to suspect

  • Recommendation 1

    Detailed patient history, a thorough clinical evaluation, identification of characteristic findings
  • Recommendation 2

    elevated levels of growth hormone or IGF-1 (insulin growth factor) .

How to test

  • Recommendation 1

    Detailed patient history, a thorough clinical evaluation, identification of characteristic findings
  • Recommendation 2

    elevated levels of growth hormone or IGF-1 (insulin growth factor) .

ZebraMD is partnering with Ambry Genetics for clinical-grade whole genome testing for rare diseases. Ambry accepts insurance. If you don’t have a physician to order this test, join our referral list and our team will reach out.

Treatment

  • Recommendation 1

    Transsphenoidal surgery for pituitary removal

Primary care

  • Recommendation 1

    Ocretoride (somatostatin analog), bromocriptine and cabergoline (dopamine agonist), pegvisomat (GH antagonist)

Further support

  • Recommendation 1

    ~ 3000 physicians . Referral to Medical Genetics Department, if available. Initial virtual care is also available through organizations like TeleRare Health.

Clinical trials

Clinical Trials

Sources

No data available

Interested in learning more about Acromegaly?

Follow to receive regular updates to the latest research development on this disease via email newsletter.