<rss version="2.0" xmlns:dc="http://purl.org/dc/elements/1.1/">
<channel>
<title>OWL: OCOSH Classification/Bone Diseases/Bone Developmental Diseases/Gigantism</title>
<link>http://www.orthopaedicweblinks.com</link>
<description>Gigantism
OCOSH Code C05.116.099.492_bd_dbd_gi</description>
<language>en-us</language>
<lastBuildDate>Thu Feb 21 2008 22:43:22 GMT</lastBuildDate>
<copyright>Copyright 2005 OWL Inc.</copyright>
<managingEditor>orthopaedicweblinks@gmail.com (Christian Veillette)</managingEditor>
<webMaster>orthopaedicweblinks@gmail.com (OWL Inc.)</webMaster>
<item>
<title>Bilateral slipped capital femoral epiphysis occuring in an adult with acromegalic gigantism</title>
<link>http://www.orthopaedicweblinks.com/Detailed/10079.html</link>
<description>Abstract
The etiology of slipped capital femoral epiphysis is still unknown. Traumatic, endocrine, toxic, and mechanical causes have all been hypothesized. It is well documented that the highest incidence occurs during the adolescent growth spurt, suggesting the role of an endocrine abnormality. We report a case that supports this hypothesis
Skeletal Radiology Volume 26, Number 3 / March, 1997
Authors
A. Feydy, R. Y. Carlier, D. Mompoint, G. Rougereau, A. Patel, C. Vallée </description>
<pubDate>2006-11-16 22:43:22 GMT</pubDate>
<guid isPermaLink="false">http://www.orthopaedicweblinks.com/cgi-bin/owl/jump.cgi?ID=10079</guid>
<author>Feydy et al</author>
</item><item>
<title>Dwarfism and gigantism in historical picture postcards</title>
<link>http://www.orthopaedicweblinks.com/Detailed/10081.html</link>
<description>Abstract
A collection of 893 historical picture postcards from 1900 to 1935, depicting dwarfs and giants, was analysed from medical and psychosocial viewpoints. In conditions such as &#039;bird headed dwarfism&#039;, achondroplasia, cretinism, so-called Aztecs or pinheads, Grebe chondrodysplasia, and acromegalic gigantism, the disorder could be diagnosed easily. In hypopituitary dwarfism, exact diagnosis was more difficult because of heterogeneity. The most common conditions depicted were pituitary dwarfism and achondroplasia. Most of those with gigantism had pituitary gigantism and acromegaly. Brothers and sisters or parents and their children provided evidence of mendelian inheritance of some of these disorders. The cards suggest that being put on show provided, at least in some cases, social benefits.
Full text available
A Enderle J R Soc Med. 1998 May; 91(5): 273–278.</description>
<pubDate>2006-11-16 22:43:22 GMT</pubDate>
<guid isPermaLink="false">http://www.orthopaedicweblinks.com/cgi-bin/owl/jump.cgi?ID=10081</guid>
<author>A Enderle</author>
</item><item>
<title>Gigantism and Acromegaly eMedicine</title>
<link>http://www.orthopaedicweblinks.com/Detailed/10078.html</link>
<description>Article by Robert Ferry MD</description>
<pubDate>2006-11-16 22:43:22 GMT</pubDate>
<guid isPermaLink="false">http://www.orthopaedicweblinks.com/cgi-bin/owl/jump.cgi?ID=10078</guid>
<author></author>
</item><item>
<title>Gigantism PubMed Search</title>
<link>http://www.orthopaedicweblinks.com/Detailed/10082.html</link>
<description>Search String
&quot;gigantism&quot;[MeSH Terms]</description>
<pubDate>2006-11-16 22:43:22 GMT</pubDate>
<guid isPermaLink="false">http://www.orthopaedicweblinks.com/cgi-bin/owl/jump.cgi?ID=10082</guid>
<author>Myles Clough</author>
</item><item>
<title>Overgrowth management in Klippel-Trenaunay-Weber and proteus syndromes</title>
<link>http://www.orthopaedicweblinks.com/Detailed/10080.html</link>
<description>Abstract
Twenty-eight patients with limb overgrowth and the diagnosis of Klippel-Trenaunay-Weber or Proteus syndromes were evaluated retrospectively. These disorders are part of the phakomatosis spectrum of syndromes. The orthopedic problems consisted of asymmetric limb overgrowth, localized gigantism, angular deformities, scoliosis, vascular malformations, and skin anomalies. Systemic abnormalities are common and deserve full evaluation before treatment. Surgical treatment consisted of epiphysiodesis, osteotomies, debulking procedures, and amputation. Mixed results were obtained with surgery, and conservative or supportive treatment should be the primary mode of orthopedic care
GUIDERA K. J. (1) ; BRINKER M. R. ; KOUSSEFF B. G. ; HELAL A. A. (1) ; PUGH L. I. (1) ; GANEY T. M. (1) ; OGDEN J. A. (1) ;
Journal of pediatric orthopedics  1993, vol. 13, no 4, pp. 538-554 (38 ref.), pp. 459-466</description>
<pubDate>2006-11-16 22:43:22 GMT</pubDate>
<guid isPermaLink="false">http://www.orthopaedicweblinks.com/cgi-bin/owl/jump.cgi?ID=10080</guid>
<author>Guidera et al</author>
</item>
</channel>
</rss>