Gigantism
You don't need to be Editor-In-Chief to add or edit content to WikiDoc. You can begin to add to or edit text on this WikiDoc page by clicking on the edit button at the top of this page. Next enter or edit the information that you would like to appear here. Once you are done editing, scroll down and click the Save page button at the bottom of the page.
| Gigantism Classification and external resources | |
| Anna Haining Bates with her parents | |
| ICD-10 | E22.0, E34.4 |
| ICD-9 | 253.0 |
| DiseasesDB | 30730 |
| MedlinePlus | 001174 |
| MeSH | D005877 |
|
WikiDoc Resources for Gigantism | |
|
Articles | |
|---|---|
|
Most recent articles on Gigantism | |
|
Media | |
|
Evidence Based Medicine | |
|
Clinical Trials | |
|
Ongoing Trials on Gigantism at Clinical Trials.gov Clinical Trials on Gigantism at Google
| |
|
Guidelines / Policies / Govt | |
|
US National Guidelines Clearinghouse on Gigantism
| |
|
Books | |
|
News | |
|
Commentary | |
|
Definitions | |
|
Patient Resources / Community | |
|
Patient resources on Gigantism Discussion groups on Gigantism Directions to Hospitals Treating Gigantism Risk calculators and risk factors for Gigantism
| |
|
Healthcare Provider Resources | |
|
Causes & Risk Factors for Gigantism | |
|
Continuing Medical Education (CME) | |
|
International | |
|
| |
|
Business | |
|
Experimental / Informatics | |
Please Take Over This Page and Apply to be Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [1] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.
Overview
Gigantism, also known as giantism (from Greek gigas, gigantas "giant"), is a condition characterized by excessive growth and height significantly above average.[1]
Types
As a medical term, gigantism can refer to:
- "Pituitary gigantism",these are people who their hormones over produce which is due to prepubertal growth hormone excess. This is sometimes equated with acromegaly, but more precisely, an excess of growth hormone leads to "pituitary gigantism" (vertical growth) if the epiphyseal plates have not yet closed,[2] but it leads to "acromegaly" (lateral growth) if they have closed.
- "Cerebral gigantism", also known as Sotos syndrome,[3] which is due to a mutation in NSD1.
Terminology
The term is typically applied to those whose height is not just in the upper 1% of the population but several standard deviations above mean for persons of the same sex, age, and ethnic ancestry. The term is seldom applied to those who are simply "tall" or "above average" whose heights appear to be the healthy result of normal genetics and nutrition.
Other names somewhat obsolete for this pathology are hypersomia (Greek: hyper over the normal level; soma body) and somatomegaly (Greek; soma body, object pronoun somatos of the body; megas, megalos great).
Many of those who have been identified with gigantism have suffered from multiple health problems involving their circulatory or skeletal system.
See also
References
External links
de:Riesenwuchs et:Gigantism el:Γιγαντισμόςeu:Erraldoitasunid:Gigantisme it:Gigantismohe:ענקיותsr:Gigantizam fi:Jättikasvu sv:Gigantism
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

