Skip Navigation

skip navigationNIDDK Home
NIDDK Reference Collection
Diet   Exercise   Health  
Home Page
-  

FAQ

Detailed Search

- -
NIDDK INFORMATION SERVICES
- -

Diabetes

Digestive Diseases

Endocrine and Metabolic Diseases

Hematologic Diseases

Kidney and Urologic Diseases

Weight-control Information Network

-
NIDDK EDUCATION
PROGRAMS

- -

National Diabetes Education Program

National Kidney Disease Education Program

-
- - -
NIDDK Home
-
Contact Us
-
New Search
-
Topic: endocrine & metabolic diseases (en)
Title: Acromegaly.
Author: n/a
Source: Bethesda, MD: National Endocrine and Metabolic Diseases Information Service. 2008. 10 p.
Availability: Available from National Endocrine and Metabolic Diseases Information Service. 6 Information Way, Bethesda, MD 20892. Phone: 1-888-828-0904. Email: endoandmeta@info .niddk.nih.gov. Website: www.endocrine.niddk.nih.gov. Price: Single copy available free of charge. Order No. EMI-1.
Abstract: This fact sheet, from the National Endocrine and Metabolic Diseases Information Service (NEMDIS), describes acromegaly, a hormonal disorder that results from too much growth hormone (GH) in the body. Usually, the excess GH comes from benign, or noncancerous, tumors on the pituitary gland. The fact sheet is written in a question-and-answer format and covers the causes of acromegaly, the symptoms of this disorder, pituitary and nonpituitary tumors, the incidence of acromegaly, diagnostic tests used to confirm the condition, and treatment options, including surgical removal of the tumor, medical therapy, and radiation therapy of the pituitary. Common features of acromegaly include abnormal growth of the hands and feet; bone growth in the face that leads to a protruding lower jaw and brow and an enlarged nasal bone; joint aches; thick, coarse, oily skin; and enlarged lips, nose, and tongue. Acromegaly can cause sleep apnea, fatigue and weakness, headaches, impaired vision, menstrual abnormalities in women, and erectile dysfunction in men. Acromegaly is diagnosed through a blood test. Magnetic resonance imaging (MRI) of the pituitary is then used to locate and detect the size of the tumor causing GH overproduction. The fact sheet concludes with a list of three resource organizations through which readers can get more information and a brief description of the activities of the NEMDIS. 1 figure. 9 references.

Format: Factsheet
Language: English.
Major Keywords: Endocrine Diseases and Disorders. Symptoms. Diagnosis. Therapy. Patient Care Management. Complications. Hypothyroidism.
Minor Keywords: Diagnostic Tests. Hormones. TSH. Thyroid Gland. Autoimmune Diseases. Hashimoto's Disease. Information Resources. Pregnancy. Etiology.
Publication Number: ENDC10131
Printer-Friendly Version | Return to Search Results
<-- previous record | next record -->

View NIDDK Publications | NIDDK Health Information | Contact Us

The NIDDK Reference Collection is a service of the National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health.
NIDDK Clearinghouses Publications Catalog
5 Information Way
Bethesda, MD 20892–3568
Phone: 1–800–860–8747
TTY: 1–866–569–1162
Fax: 703–738–4929
Email: catalog@niddk.nih.gov

Privacy | Disclaimers | Accessibility | Public Use of Materials
H H S logo - link to U. S. Department of Health and Human Services NIH logo - link to the National Institute of Health NIDDK logo - link to the National Institute of Diabetes and Digestive and Kidney Diseases