McCune-Albright Syndrome

 

 

Growth Hormone

 

Excessive secretion of pituitary growth hormone has been seen in a few patients with McCune-Albright syndrome. Most of these have been diagnosed as young adults, when they developed the coarsening of facial features, enlargement of hands and feet, and arthritis characteristic of the condition termed acromegaly. Therapy has included surgical removal of the area of the pituitary which is secreting the hormone, and the use of new, synthetic analogs of the hormone somatostatin, which suppress growth hormone secretion.
 

 

 

 

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