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acromegaly

acromegaly

acromegaly Sentence Examples

  • Somatostatin analogs, given as injections, are successful in treating acromegaly by inhibiting the release of GH.

  • In adults, too much GH causes a condition called acromegaly, but deficiency in adults had been considered previously to have no importance.

  • Many of the characteristics portrayed are the consequences of untreated acromegaly.

  • antagonist for the treatment of the abnormal growth condition acromegaly where conventional treatments have failed.

  • There are conditions in which we have an abnormal increase in the tissue elements but which strictly should not be defined as hypertrophies, such as new-growths, abnormal enlargements of bones and organs due to syphilis, tuberculosis, osteitis deformans, acromegaly, myxoedema, &c. The enormously long teeth sometimes found in rodents also are not due to hypertrophy, as they are normally endowed with rapid growth to compensate for the constant and rapid attrition which takes place from the opposed teeth.

  • of suprarenal capsule in Addison's disease, of bone marrow in pernicious anaemia, of thymus and suprarenal capsule in exophthalmic goitre, of kidney in renal disease, and of pituitary body in acromegaly.

  • Overproduction of hGH or IGH-I, or an exaggerated response to these hormones, can lead to gigantism or acromegaly, both of which are characterized by a very large stature.

  • Acromegaly results when hGH is over-produced after the onset of puberty.

  • The somatotropin test also aids in documenting the excess hGH production responsible for gigantism or acromegaly, and confirms underactivity or overproduction of the pituitary gland (hypopituitarism or hyperpituitarism, respectively).

  • The somatomedin C test is usually ordered to help detect pituitary abnormalities, hGH deficiency, and acromegaly.

  • This procedure, also called the glucose loading test, is performed to evaluate excessive baseline levels of hGH and to confirm diagnosis of gigantism in children (and acromegaly in adults).

  • In a child with excessive hGH levels, failure of suppression indicates anterior pituitary dysfunction and confirms a diagnosis of gigantism (or acromegaly).

  • If such a tumor develops within the first ten years of life, the result is gigantism (in which growth is accelerated) and not acromegaly.

  • If the tumor develops after growth has stopped, the result is acromegaly, not gigantism.

  • If the tumor develops after growth has stopped, the result is acromegaly, not gigantism.

  • Acromegaly is a disease in which an abnormality in the pituitary gland leads to an oversecretion of growth hormone.

  • Acromegaly is a disorder in which the abnormal release of a particular chemical from the pituitary gland in the brain causes increased growth in bone and soft tissue, as well as a variety of other disturbances throughout the body.

  • In children whose bony growth plates have not closed, the chemical changes of acromegaly result in exceptional growth of long bones.

  • When the abnormality occurs after bone growth stops, i.e. in adults, the disorder is called acromegaly.

  • Acromegaly is a relatively rare disorder, occurring in approximately 50 out of every 1 million people.

  • The cause of acromegaly can be traced to the pituitary's production of GH.

  • In acromegaly, the pituitary continues to release GH and ignores signals from the hypothalamus.

  • The most common cause of acromegaly and gigantism is the development of a noncancerous tumor within the pituitary, called a pituitary adenoma.

  • In rare cases, acromegaly is caused by the abnormal production of GHRH, which leads to the increased production of GH.

  • In acromegaly, an individual's hands and feet begin to grow, becoming thick and doughy.

  • People with acromegaly have more skin tags, or outgrowths of tissue, than normal.

  • Patients with acromegaly often suffer from headaches and arthritis.

  • Because acromegaly produces slow changes, diagnosis is often significantly delayed.

  • Because the quantity of GH produced varies widely under normal conditions, demonstrating high levels of GH in the blood is not sufficient to merit a diagnosis of acromegaly.

  • Patients with acromegaly will not show this decrease and will often show an increase in GH production.

  • The first step in treatment of acromegaly is removal of all or part of the pituitary adenoma.

  • While this surgery can cause rapid improvement of many acromegaly symptoms, most patients will also require additional treatment with medication.

  • Individuals with acromegaly or gigantism who have diabetes or diabetes-like symptoms should maintain a diet that helps normalize blood sugar levels.

  • Without treatment, patients with acromegaly are likely to die early because of the disease's effects on the heart, lungs, brain, or due to the development of cancer in the large intestine.

  • With treatment, however, a patient with acromegaly may be able to live a normal lifespan.

  • The initial onset of acromegaly or gigantism cannot as of 2004 be prevented.

  • "Acromegaly." In Williams Textbook of Endocrinology, 10th ed. Edited by P.

  • Melmed, Shlomo, et al. "Consensus Guidelines for Acromegaly Management."

  • "Gigantism and Acromegaly." eMedicine, July 29, 2004.

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