Acromegaly overview: Difference between revisions
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==Overview== | |||
'''Acromegaly''' (from Greek ''akros'' "extreme" or "extremities" and ''megalos'' "large" - extremities enlargement) is a [[hormone|hormonal]] disorder that results when the [[pituitary]] gland produces excess [[human growth hormone|growth hormone]] (hGH). Most commonly it begins when a GH producing tumor derived from a distinct type of cells ([[somatotrophs]]) and called '''[[pituitary adenoma]]'''. | |||
Acromegaly most commonly affects middle-aged adults and can result in serious illness and premature death. Because of its insidious pathogenesis and slow progression, the disease is hard to diagnose in the early stages and is frequently missed for many years. | |||
==References== | ==References== | ||
Revision as of 15:28, 18 January 2012
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Acromegaly Microchapters |
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Acromegaly overview On the Web |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Acromegaly (from Greek akros "extreme" or "extremities" and megalos "large" - extremities enlargement) is a hormonal disorder that results when the pituitary gland produces excess growth hormone (hGH). Most commonly it begins when a GH producing tumor derived from a distinct type of cells (somatotrophs) and called pituitary adenoma.
Acromegaly most commonly affects middle-aged adults and can result in serious illness and premature death. Because of its insidious pathogenesis and slow progression, the disease is hard to diagnose in the early stages and is frequently missed for many years.
References
bg:Акромегалия cs:Akromegalie de:Akromegalie gl:Acromegalia it:Acromegalia he:אקרומגליה nl:Acromegalie no:Akromegali sq:Akromegalia sk:Akromegália sr:Акромегалија fi:Akromegalia sv:Akromegali uk:Акромегалія