enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Acromegaly - Wikipedia

    en.wikipedia.org/wiki/Acromegaly

    The latest development in the medical treatment of acromegaly is the use of growth hormone receptor antagonists. The only available member of this family is pegvisomant (Somavert). By blocking the action of the endogenous growth hormone molecules, this compound is able to control the disease activity of acromegaly in virtually everyone with ...

  3. Pegvisomant - Wikipedia

    en.wikipedia.org/wiki/Pegvisomant

    Pegvisomant, sold under the brand name Somavert, is a growth hormone receptor antagonist used in the treatment of acromegaly. [1] [2] [3] It is primarily used if the pituitary gland tumor causing the acromegaly cannot be controlled with surgery or radiation, and the use of somatostatin analogues is unsuccessful, but is also effective as a monotherapy. [4]

  4. Growth hormone therapy - Wikipedia

    en.wikipedia.org/wiki/Growth_hormone_therapy

    This article describes the history of GH treatment and the current uses and risks arising from GH use. Other articles describe GH physiology, diseases of GH excess (acromegaly and pituitary gigantism), deficiency, the recent phenomenon of HGH controversies, growth hormone in sports, and growth hormone for cows.

  5. Hyperpituitarism - Wikipedia

    en.wikipedia.org/wiki/Hyperpituitarism

    Hyperpituitarism is a condition due to the primary hypersecretion of pituitary hormones; [3] [medical citation needed] it typically results from a pituitary adenoma.In children with hyperpituitarism, disruption of growth regulation is rare, either because of hormone hypersecretion or because of manifestations caused by local compression of the adenoma.

  6. Cushing's disease - Wikipedia

    en.wikipedia.org/wiki/Cushing's_disease

    External-beam pituitary RT is more effective treatment for pediatric CD in children with cure rates of 80–88%. Hypopituitarism specifically growth hormone deficiency has been reported as the only most common late morbidity of this treatment; GHD has been reported in 36% and 68% of the patients undergoing post-pituitary RT for Cushing's ...

  7. Osteoporosis - Wikipedia

    en.wikipedia.org/wiki/Osteoporosis

    Some professional guidelines recommend prophylaxis in patients who take the equivalent of more than 30 mg hydrocortisone (7.5 mg of prednisolone), especially when this is in excess of three months. [75] It is recommended to use calcium or Vitamin D as prevention. [76] Alternate day use may not prevent this complication. [77]

  8. Somatostatin - Wikipedia

    en.wikipedia.org/wiki/Somatostatin

    It is indicated for symptomatic treatment of carcinoid syndrome and acromegaly. [ 22 ] [ 23 ] It is also finding increased use in polycystic diseases of the liver and kidney. Lanreotide (Somatuline, Ipsen Pharmaceuticals ) is a medication used in the management of acromegaly and symptoms caused by neuroendocrine tumors, most notably carcinoid ...

  9. Growth hormone deficiency - Wikipedia

    en.wikipedia.org/wiki/Growth_hormone_deficiency

    In many countries, including the UK, the majority view among endocrinologists is that the failure of treatment to provide any demonstrable, measurable benefits in terms of outcomes means treatment is not recommended for all adults with severe GHD, [25] and national guidelines in the UK as set out by NICE suggest three criteria which all need to ...