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Acromegaly: more books (50)

The Pituitary Patient Resource Guide, 3rd Edition by Shereen Ezzat, 2001-12-01

The Pituitary Patient Resource Guide, 4th Ed. (It Is All In Your Head! (CD/PDF format))

The Pituitary Patient Resource Guide, 4th Ed. (It Is All In Your Head!)

Standing Tall: Unusually Tall People (First Book) by Elaine Landau, 1997-04

The Jewish Giant by Stacy Abramson, 2000-03-28

A case of agromegaly, and illustrations of two allied conditions by Frederick Adolphus Packard, 1892

Acromegalia;: From the Pathological Institute of the New York state hospitals by Harlow Brooks, 1899

The apologia of an acromegalic by Leonard Portal Mark, 1927

lists with details

Acromegaly
Endocrinology. acromegaly. What is acromegaly? Untreated, the disease canlead to severe illness and death. What are the symptoms of acromegaly?
http://www.mcghealthcare.org/endocrinology/pithub/acromegaly/acromegaly.htm

Extractions: Acromegaly is the Greek word for "extremities" and "enlargement." When the pituitary gland produces excess growth hormones, this results in excessive growth, called acromegaly. The excessive growth occurs first in the hands and feet, as soft tissue begins to swell. Acromegaly affects mostly middle-aged adults. Untreated, the disease can lead to severe illness and death. What are the symptoms of acromegaly? Symptoms of acromegaly vary depending on how long the patient has had the disease. The following are the most common symptoms. However, each individual may experience symptoms differently: swelling of the hands and feet facial features become course as bones grow body hair becomes course as the skin thickens and/or darkens increased perspiration accompanied with body odor protruding jaw voice deepening enlarged lip, nose, and tongue
Healthology Acromegaly
Sign Up For acromegaly Updates . acromegaly acromegaly.
http://www.advancesinoncology.com/focus_index.asp?f=aio_acromegaly
MDchoice.com The Ultimate Medical Information Finder Acromegaly
page. acromegaly. height. What Causes acromegaly? acromegaly is causedby prolonged overproduction of GH by the pituitary gland.
http://mdchoice.com/Pt/consumer/acromegaly.asp

Extractions: of the Health On the Net Foundation Spell Checker Search the Web's best medical sites Searches over 6,000 Medical Journals Health Information Sunday, March 30, 2003 Find more information about this topic from either the Web or the world's best medical journals by using the search boxes at the top of this page. Acromegaly Acromegaly is a hormonal disorder that results when the pituitary gland produces excess growth hormone (GH). It most commonly affects middle-aged adults and can result in serious illness and premature death. Once recognized, acromegaly is treatable in most patients, but because of its slow and often insidious onset, it frequently is not diagnosed correctly. The name acromegaly comes from the Greek words for "extremities" and "enlargement" and reflects one of its most common symptoms, the abnormal growth of the hands and feet. Soft tissue swelling of the hands and feet is often an early feature, with patients noticing a change in ring or shoe size. Gradually, bony changes alter the patient's facial features: the brow and lower jaw protrude, the nasal bone enlarges, and spacing of the teeth increases.
AACE Program Advances Care Of Acromegaly
AACE Program Advances Care of acromegaly JACKSONVILLE, Fla., May 2, 1996 Workingfrom the premise that treating a rare disorder should not be hampered by
http://www.pslgroup.com/dg/82BA.htm
Acromegaly. The Columbia Encyclopedia, Sixth Edition. 2001
2001. acromegaly. acromegaly is usually caused by a tumor of the pituitary;treatment consists of irradiation or surgical removal of the tumor.
http://www.bartleby.com/65/ac/acromega.html

Extractions: Select Search All Bartleby.com All Reference Columbia Encyclopedia World History Encyclopedia World Factbook Columbia Gazetteer American Heritage Coll. Dictionary Roget's Thesauri Roget's II: Thesaurus Roget's Int'l Thesaurus Quotations Bartlett's Quotations Columbia Quotations Simpson's Quotations English Usage Modern Usage American English Fowler's King's English Strunk's Style Mencken's Language Cambridge History The King James Bible Oxford Shakespeare Gray's Anatomy Farmer's Cookbook Post's Etiquette Bulfinch's Mythology Frazer's Golden Bough All Verse Anthologies Dickinson, E. Eliot, T.S. Frost, R. Hopkins, G.M. Keats, J. Lawrence, D.H. Masters, E.L. Sandburg, C. Sassoon, S. Whitman, W. Wordsworth, W. Yeats, W.B. All Nonfiction Harvard Classics American Essays Einstein's Relativity Grant, U.S. Roosevelt, T. Wells's History Presidential Inaugurals All Fiction Shelf of Fiction Ghost Stories Short Stories Shaw, G.B. Stein, G. Stevenson, R.L. Wells, H.G. Reference Columbia Encyclopedia PREVIOUS NEXT ... BIBLIOGRAPHIC RECORD The Columbia Encyclopedia, Sixth Edition. acromegaly m l KEY ) , adult endocrine disorder resulting from hypersecretion of growth hormone produced by the pituitary gland. Since the bones cannot increase in length after full growth is attained, there is a disproportionate thickening of bones, predominantly in the skull and small bones of the hands and feet. Fingers and toes become broadened and spadelike, the skull increases in size, and the cheek bones and jaws protrude. Many of the soft tissues, such as the tongue and liver, enlarge. Frequently glucose metabolism is disturbed, leading to diabetes mellitus. Acromegaly is usually caused by a tumor of the pituitary; treatment consists of irradiation or surgical removal of the tumor. Onset of the disease can also occur in children, before the epiphyses of the bones are closed. In such cases the disorder leads to
Acromegaly. The American Heritage® Dictionary Of The English Language: Fourth Ed
acromegaly. The American Heritage® Dictionary of the English Language FourthEdition. 2000. 2000. acromegaly. SYLLABICATION ac·ro·meg·a·ly.
http://www.bartleby.com/61/53/A0065300.html

Extractions: Select Search All Bartleby.com All Reference Columbia Encyclopedia World History Encyclopedia World Factbook Columbia Gazetteer American Heritage Coll. Dictionary Roget's Thesauri Roget's II: Thesaurus Roget's Int'l Thesaurus Quotations Bartlett's Quotations Columbia Quotations Simpson's Quotations English Usage Modern Usage American English Fowler's King's English Strunk's Style Mencken's Language Cambridge History The King James Bible Oxford Shakespeare Gray's Anatomy Farmer's Cookbook Post's Etiquette Bulfinch's Mythology Frazer's Golden Bough All Verse Anthologies Dickinson, E. Eliot, T.S. Frost, R. Hopkins, G.M. Keats, J. Lawrence, D.H. Masters, E.L. Sandburg, C. Sassoon, S. Whitman, W. Wordsworth, W. Yeats, W.B. All Nonfiction Harvard Classics American Essays Einstein's Relativity Grant, U.S. Roosevelt, T. Wells's History Presidential Inaugurals All Fiction Shelf of Fiction Ghost Stories Short Stories Shaw, G.B. Stein, G. Stevenson, R.L. Wells, H.G. Reference American Heritage Dictionary acrolein ... BIBLIOGRAPHIC RECORD The American Heritage Dictionary of the English Language: Fourth Edition. acromegaly SYLLABICATION: PRONUNCIATION k r -m g -l NOUN: A chronic disease of adults marked by enlargement of the bones of the extremities, face, and jaw that is caused by overactivity of the pituitary gland.
Acromegaly & Octreotide
Neuroendocrine Clinical HomeMedical Management of acromegalywith Octreotide by Larry Katznelson, MD.
http://neurosurgery.mgh.harvard.edu/NeuroEndocrine/E-F-943.HTM

Extractions: Guestbook Neurosurgery Home ... Links The pulsatile release of growth hormone (GH) by normal somatotroph cells is regulated by growth hormone releasing hormone (GHRH), which stimulates GH secretion, and somatostatin, which decreases secretion. At the liver, GH stimulates secretion of somatomedin C, also known as insulin-like growth factor 1 (IGF-1), which mediates many of the peripheral somatic effects of GH. IGF-1 feeds back at the level of the hypothalamus and pituitary resulting in a reduction in GH secretion. The diagnosis of acromegaly is based on three key findings: 1) clinical evidence, 2) demonstration of an elevated IGF-1 level, and 3) inability to suppress serum GH to less than 2 ng/ml following an oral glucose challenge (OGTT). In patients who do not have a significant reduction in GH levels in response to intermittent octreotide injections, more frequent dosing of octreotide may result in a greater clinical response. Octreotide may be administered continuously by a subcutaneous pump to patients with refractory acromegaly to prevent escape of GH between injections. In addition, studies using a long-acting injectable form of octreotide that is administered once a month are underway in Europe and are likely to be initiated here in the near future.
Welcome To ENH.org - Health Encyclopedia: Acromegaly
acromegaly. Definition acromegaly is a chronic metabolic disordercaused by the presence of too much growth hormone. It results
http://www.enh.org/Encyclopedia/ency/article/000321.asp

Extractions: Disease Reference Injury Reference Test Reference Nutrition Reference ... Symptoms Reference Disease Injury Nutrition Poison ... Z Definition: Acromegaly is a chronic metabolic disorder caused by the presence of too much growth hormone. It results in gradual enlargement of body tissues including the bones of the face, jaw, hands, feet, and skull. Causes, incidence, and risk factors: Acromegaly occurs in about 6 of every 100,000 adults. It is caused by abnormal production of growth hormone after normal growth of the skeleton and other organs is complete. Excessive production of growth hormone in children causes gigantism rather than acromegaly. The cause of the increased hormone secretion is usually a benign tumor of the pituitary gland. The pituitary gland, which is located just below the brain, controls the production and release of several different hormones including growth hormone. There are no known risk factors for acromegaly other than a prior history of a pituitary tumor.
Acromegaly & Octreotide
Medical Management of acromegaly with Octreotide by Larry Katznelson, MD.
http://pituitary.mgh.harvard.edu/e-f-943.htm

Extractions: Guestbook Neurosurgery Home ... Links The pulsatile release of growth hormone (GH) by normal somatotroph cells is regulated by growth hormone releasing hormone (GHRH), which stimulates GH secretion, and somatostatin, which decreases secretion. At the liver, GH stimulates secretion of somatomedin C, also known as insulin-like growth factor 1 (IGF-1), which mediates many of the peripheral somatic effects of GH. IGF-1 feeds back at the level of the hypothalamus and pituitary resulting in a reduction in GH secretion. The diagnosis of acromegaly is based on three key findings: 1) clinical evidence, 2) demonstration of an elevated IGF-1 level, and 3) inability to suppress serum GH to less than 2 ng/ml following an oral glucose challenge (OGTT). In patients who do not have a significant reduction in GH levels in response to intermittent octreotide injections, more frequent dosing of octreotide may result in a greater clinical response. Octreotide may be administered continuously by a subcutaneous pump to patients with refractory acromegaly to prevent escape of GH between injections. In addition, studies using a long-acting injectable form of octreotide that is administered once a month are underway in Europe and are likely to be initiated here in the near future.
Acromegaly And Gigantism
acromegaly and gigantism. In children whose bony growth plates have not closed, thechemical changes of acromegaly result in exceptional growth of long bones.
http://www.healthatoz.com/healthatoz/Atoz/ency/acromegaly_and_gigantism.html

Extractions: Definition 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. This chemical released from the pituitary gland is called growth hormone (GH). The body's ability to process and use nutrients like fats and sugars is also altered. In children whose bony growth plates have not closed, the chemical changes of acromegaly result in exceptional growth of long bones. This variant is called gigantism, with the additional bone growth causing unusual height. When the abnormality occurs after bone growth stops, the disorder is called acromegaly. Description Acromegaly is a relatively rare disorder, occurring in approximately 50 out of every one million people (50/1,000,000). Both men and women are affected. Because the symptoms of acromegaly occur so gradually, diagnosis is often delayed. The majority of patients are not identified until they are middle aged. Causes and symptoms The pituitary is a small gland located at the base of the brain. A gland is a collection of cells that releases certain chemicals, or hormones, which are important to the functioning of other organs or body systems. The pituitary hormones travel throughout the body and are involved in a large number of activities, including the regulation of growth and reproductive functions. The cause of acromegaly can be traced to the pituitary's production of GH.
SupportPath.com: Acromegaly
SupportPath.com, acromegaly. Other topics of interest on SupportPath.comRare Disorders. Clinical Trials Research on acromegaly
http://www.supportpath.com/sl_a/acromegaly.htm

Extractions: Description: Their Mission: "To support, pursue, encourage, promote and where possible, fund research on pituitary tumors and related pituitary disorders in a sustained and full-time effort to find a cure for these illnesses." Website features include bulletin boards, links, articles on diseases, and a glossary of terms.
Health Library Find Information On Acromegaly At MerckSource
Find information on acromegaly at MerckSource. Learn more about acromegaly,acromegaly acromegaly. Definition acromegaly is a chronic metabolic
http://www.mercksource.com/pp/us/cns/cns_hl_adam.jspzQzpgzEzzSzppdocszSzuszSzcns
Acromegaly
acromegaly Guide picks. acromegaly If this growth hormone disorder begins in puberty,it causes gigantism (the wrestler Andre the Giant was affected by it).
http://rarediseases.about.com/cs/acromegaly/

Extractions: If this growth hormone disorder begins in puberty, it causes gigantism (the wrestler Andre the Giant was affected by it). Most often it begins in middle age due to a tumor of the pituitary gland and causes abnormal growth of the hands and face. From the About.com Guide to Rare/Orphan Diseases. NIDDK: Acromegaly
Endocrinology - Acromegaly
acromegaly What is acromegaly ? acromegaly affects mostly middleaged adults.Untreated, the disease can lead to severe illness and death.
http://www.stjohnsmercy.org/healthinfo/adult/endocrin/acromegaly.asp

Extractions: Acromegaly is the Greek word for "extremities" and "enlargement." When the pituitary gland produces excess growth hormones, this results in excessive growth called acromegaly. The excessive growth occurs first in the hands and feet, as soft tissue begins to swell. Acromegaly affects mostly middle-aged adults. Untreated, the disease can lead to severe illness and death. Symptoms of acromegaly vary depending on how long the patient has had the disease. The following are the most common symptoms of acromegaly. However, each individual may experience symptoms differently. Symptoms may include: swelling of the hands and feet facial features become coarse as bones grow body hair becomes coarse as the skin thickens and/or darkens increased perspiration accompanied with body odor protruding jaw voice deepening enlarged lip, nose, and tongue
Ipsen Limited - Information For Patients With Acromegaly
Information for patients with acromegaly, Company, Products, Patients, Contacts,Medical Dictionary, Links. What is acromegaly? Management of acromegaly.
http://www.ipsen.ltd.uk/patients/acromegaly/
Ipsen Limited - What Is Acromegaly?
What is acromegaly? such as diabetes. Symptoms of acromegaly. Changesin facial features, Joint stiffness, arthritis. Enlargement of
http://www.ipsen.ltd.uk/patients/acromegaly/acromegaly1.html

Extractions: Acromegaly is the term used for a rare clinical condition in adults that is caused by the prolonged, excess release of growth hormone from the pituitary gland . It affects men and women equally, and in most cases, is not hereditary, so it cannot be passed onto children. The excess release of growth hormone promotes the growth of both skeletal and soft tissues, as well as causing metabolic changes that can result in symptoms such as diabetes Symptoms of acromegaly Changes in facial features Joint stiffness, arthritis Enlargement of hands, feet, jaw (separation of teeth) Tingling in the fingers and hands (carpal tunnel syndrome) Excessive sweating and / or abnormal hairiness Ear, nose (snoring), throat or dental problems Tiredness and lethargy Some loss of vision Increased frequency and / or severity of headaches Impaired glucose tolerance or diabetes Enlargement of the thyroid gland Hypertension Irregular menstrual cycle Loss of libido Back Next - about the pituitary gland 1992-EX-11-03
Acromegaly And Gigantism
acromegaly and gigantism. In children whose bony growth plates have not closed, thechemical changes of acromegaly result in exceptional growth of long bones.
http://www.hendrickhealth.org/healthy/000015.htm

Extractions: Resources 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. This chemical released from the pituitary gland is called growth hormone (GH). The body's ability to process and use nutrients like fats and sugars is also altered. In children whose bony growth plates have not closed, the chemical changes of acromegaly result in exceptional growth of long bones. This variant is called gigantism, with the additional bone growth causing unusual height. When the abnormality occurs after bone growth stops, the disorder is called acromegaly. Acromegaly is a relatively rare disorder, occurring in approximately 50 out of every one million people (50/1,000,000). Both men and women are affected. Because the symptoms of acromegaly occur so gradually, diagnosis is often delayed. The majority of patients are not identified until they are middle aged. The pituitary is a small gland located at the base of the brain. A gland is a collection of cells that releases certain chemicals, or hormones, which are important to the functioning of other organs or body systems. The pituitary hormones travel throughout the body and are involved in a large number of activities, including the regulation of growth and reproductive functions. The cause of acromegaly can be traced to the pituitary's production of GH.
Treating Acromegaly Endocrinology Medicine J A H Wass
Treating acromegaly Endocrinology Medicine JAH Wass. Subject EndocrinologyMedicine Title Treating acromegaly Author JAH Wass.
http://www.bookssource.co.uk/J-A-H-Wass-Treating-Acromegaly-1898099057.html
Acromegaly
acromegaly. Image URL Acromegalic heart, Image URL acromegaly, ImageURL Adenoma in acromegaly, Image URL Adenoma in acromegaly,
http://www.brisbio.ac.uk/ROADS/subject-listing/acromegaly.html
Acromegaly
acromegaly acromegaly, IGFI . Serial growth hormone after 75 g oral glucoseload (growth hormone suppression test) is a satisfactory alternative.
http://www.rcpa.edu.au/pathman/acromega.htm

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