Acromegaly

Not Verified
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) .

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

  • Recommendation 1

    13 actively recruiting

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.