Geometry.Net - Health_Conditions: Ehlers-danlos Syndrome

Ivanhoe's Medical Breakthroughs - Ehlers-Danlos Syndrome -- Full-Length Expert's
Email a Friend Reported February 1, 2002 ehlers-danlos syndrome Full-Length Expert's Interview. What is ehlers-danlos syndrome?
http://www.ivanhoe.com/channels/p_channelstory.cfm?storyid=3058
NEJM A Recessive Form Of The Ehlers-Danlos Syndrome Caused By
A Recessive Form of the EhlersDanlos Syndrome Caused by TenascinX DeficiencyJoost Schalkwijk, Ph.D., Manon C. Zweers, Ph.D., Peter M. Steijlen, MD, Willow
http://content.nejm.org/cgi/content/full/345/16/1167
NEJM Ehlers-Danlos Syndrome
Next Next. EhlersDanlos Syndrome. In 1956, McKusick 6 included EhlersDanlossyndrome in the first compilation of heritable disorders of connective tissue.
http://content.nejm.org/cgi/content/full/342/10/730
UCSF News Archive: Gene Linked In Ehlers-Danlos Syndrome
Gene Linked in ehlersdanlos syndrome. FOR IMMEDIATE RELEASE May 7, 1997. UCSF RESEARCHERSFIND GENE LINKED TO CONNECTIVE TISSUE DEFECT IN ehlers-danlos syndrome.
http://www.ucsf.edu/~adcom/listserv/ucsfnews/0089.html
Ehlers-Danlos Syndrome Book From SignQuest Publishers, Inc.
A Book about ehlersdanlos syndrome. by People with ehlers-danlos syndrome. Whatis EDS? ehlers-danlos syndrome is a collection of characteristics.
http://www.massoud.org/eds.htm

Extractions: How to Contact the Company Ehlers-Danlos Syndrome is a collection of characteristics. It is not a disease to be treated, but a description of a person's "condition." EDS is a condition in which collagen, the protein that holds the body together, doesn't. A person with EDS has some combination of abnormalities in the skin, ligaments, and internal organs. In several types EDS, the abnormalities may result in additional complications to joints. Doctors Ehlers and Danlos described this hereditary condition in the early 1900s. It affects both children and adults, has various types, and is very difficult to be diagnosed. This book has been written with the help of testimonies from EDS folks and their families and although it is not a replacement for medical care or advice, it is a very helpful source of information for those who suffer from EDS or have family members and friends who have EDS. Introduction 1 Frequently Asked Questions (FAQs) 1 Medical Abbreviations 4 E-mail Abbreviations 4 Other Sources of Information about EDS 5 Format 6 Initial Miscellaneous Observations 6 Anesthetic 7 Arthritis/Joint Noises 8 Balance 10 Blood 11 Body Temperature and Pressure 12 Braces and Splints 14 Cardiac 16 Chiropractic 18 Diet 18 Dislocations/Subluxations 20 Doctor Comments/Knowledge 24 Diagnosis Stories 27
Ehlers-Danlos Syndrome
ehlersdanlos syndrome. Clinical and Genetic Features of ehlers-danlos syndromeType IV, the Vascular Type. The New England Journal of Medicine 342, no.
http://www.healthatoz.com/healthatoz/Atoz/ency/ehlers-danlos_syndrome.html

Extractions: Definition The Ehlers-Danlos syndromes (EDS) refer to a group of inherited disorders that affect collagen structure and function. Genetic abnormalities in the manufacturing of collagen within the body affect connective tissues, causing them to be abnormally weak. Description Collagen is a strong, fibrous protein that lends strength and elasticity to connective tissues such as the skin, tendons, organ walls, cartilage, and blood vessels. Each of these connective tissues requires collagen tailored to meet its specific purposes. The many roles of collagen are reflected in the number of genes dedicated to its production. There are at least 28 genes in humans that encode at least 19 different types of collagen. Mutations in these genes can affect basic construction as well as the fine-tuned processing of the collagen. EDS was originally described by Dr. Van Meekeren in 1682. Dr. Ehlers and Dr. Danlos further characterized the disease in 1901 and 1908, respectively. Today, according to the Ehlers-Danlos National Foundation, one in 5,000 to one in 10,000 people are affected by some form of EDS. EDS is a group of genetic disorders that usually affects the skin, ligaments, joints, and blood vessels. Classification of EDS types was revised in 1997. The new classification involves categorizing the different forms of EDS into six major sub-types, including classical, hypermobility, vascular, kyphoscoliosis, arthrochalasia, and dermatosparaxis, and a collection of rare or poorly defined varieties. This new classification is simpler and based more on descriptions of the actual symptoms.
Health Library - Ehlers Danlos Syndrome
Ehlers Danlos Syndrome. Synonyms. ED Syndrome; EDS. Disorder Subdivisions. EDSGravis Type (Type 1); ehlersdanlos syndrome Type II; EDS Mitis Type (Type II);
http://www.laurushealth.com/library/healthguide/illnessconditions/topic.asp?hwid
Ehlers-Danlos Syndrome From Pediatrics / Genetics And Metabolic Disease
eMedicine Journal Pediatrics Genetics And Metabolic Disease ehlersdanlos syndromeSynonyms, Key Words, and Related Terms EDS, connective tissue disorders
http://author.emedicine.com/ped/topic654.htm

Extractions: Synonyms, Key Words, and Related Terms: EDS, connective tissue disorders, joint laxity, articular hypermobility, skin laxity, hyperextensible skin, abnormal wound healing, hypermobility syndrome, collagen abnormalities, lysyl hydroxylase deficiency, periodontitis, fibronectin, platelet aggregation defect, acrogeria, tissue fragility, vascular rupture, colonic perforation, excessive bruising, easy bruising, prominent venous plexus, petechiae, retinal detachment, dystrophic scarring Author Information Introduction Clinical Differentials ... Bibliography AUTHOR INFORMATION Section 1 of 11 Authored by G Bradley Schaefer, MD , Director of Hattie B Munroe Center for Human Genetics, Professor, Department of Pediatrics, University of Nebraska Medical Center G Bradley Schaefer, MD, is a member of the following medical societies: American Academy of Pediatrics , and American College of Medical Genetics Edited by Michael Fasullo, PhD , Associate Professor, Center for Immunology and Microbial Disease, Albany Medical College;
Health Library - Ehlers Danlos Syndrome
Ehlers Danlos Syndrome. Self Help Clearinghouse. 25 branches. Founded 1985.Emotionalsupport and updated information to persons with ehlersdanlos syndrome.
http://yalenewhavenhealth.org/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc29e
EDS Information
EDS Today. The newsletter for, by, and about people with EhlersDanlosSyndrome. (CEDA). ehlers-danlos syndrome. ehlers-danlos syndrome.
http://www.edstoday.org/links.htm
Health Library - Ehlers Danlos Syndrome
Saint Luke's Health System eLibrary. Ehlers Danlos Syndrome. EDS GravisType (Type 1); ehlersdanlos syndrome Type II; EDS Mitis Type (Type II);
http://hvelink.saint-lukes.org/library/healthguide/IllnessConditions/topic.asp?h
Ehlers-Danlos Syndrome
ehlersdanlos syndrome. Pathology. ehlers-danlos syndrome (EDS) isa genetic disorder caused by the incorect folding of Collagen.
http://www.diseasedir.org.uk/genetic/gene0101.htm

Extractions: Chromosomes: Pathology Ehlers-Danlos Syndrome (EDS) is a genetic disorder caused by the incorect folding of Collagen. Collagen is a vital component of most tissues. It consists of three collagen strands wrapped into a triple helix Collagen can form this triple helix by possesing a strictly defined Amino Acid sequence. In a triple helix every third Amino acid points inside of the helix, because there is not much space on the inside of the helix the smallest Amino acid must be used - Glycine The Amino Acid sequence of Collagen then follows the pattern Glycine - X - X. Where the X is another Amino Acid (These don't matter so much as they point outward from the center of the helix). Although the precise mechanism by which EDS is caused is unknown, it is thought to involve the incorrect folding of the collagen molecules. Aetiology Symptoms EDS Type I - Gravis variety. Soft, hyperextensible (very stretchy) skin easily bruised. scars over body. hypermobile joints (over-flexible joints) varicose veins.
Scientific Program - Orthopaedic Manifestations Of Ehlers-Danlos Syndrome: A New
American Academy of Orthopaedic Surgeons 1996 Annual Meeting Scientific Program.*Orthopaedic Manifestations of ehlers-danlos syndrome A New Perspective.
http://www.aaos.org/wordhtml/anmeet96/sciprog/174.htm
Ehlers-Danlos Syndrome
MAIN SEARCH INDEX ehlersdanlos syndrome. Living a Restricted Life with Ehlers-DanlosSyndrome. International Journal of Nursing Studies 37 (2000) 111-118.
http://www.hendrickhealth.org/healthy/000462.htm

Extractions: Resources The Ehlers-Danlos syndromes (EDS) refer to a group of inherited disorders that affect collagen structure and function. Genetic abnormalities in the manufacturing of collagen within the body affect connective tissues, causing them to be abnormally weak. Collagen is a strong, fibrous protein that lends strength and elasticity to connective tissues such as the skin, tendons, organ walls, cartilage, and blood vessels. Each of these connective tissues requires collagen tailored to meet its specific purposes. The many roles of collagen are reflected in the number of genes dedicated to its production. There are at least 28 genes in humans that encode at least 19 different types of collagen. Mutations in these genes can affect basic construction as well as the fine-tuned processing of the collagen. EDS was originally described by Dr. Van Meekeren in 1682. Dr. Ehlers and Dr. Danlos further characterized the disease in 1901 and 1908, respectively. Today, according to the Ehlers-Danlos National Foundation, one in 5,000 to one in 10,000 people are affected by some form of EDS. EDS is a group of genetic disorders that usually affects the skin, ligaments, joints, and blood vessels. Classification of EDS types was revised in 1997. The new classification involves categorizing the different forms of EDS into six major sub-types, including classical, hypermobility, vascular, kyphoscoliosis, arthrochalasia, and dermatosparaxis, and a collection of rare or poorly defined varieties. This new classification is simpler and based more on descriptions of the actual symptoms.
University Of Miami School Of Medicine - Glossary - Ehlers-Danlos Syndrome
Diseases and Conditions. ehlersdanlos syndrome. ehlers-danlos syndrome. Whatis ehlers-danlos syndrome? ehlers-danlos syndromes is
http://www.med.miami.edu/patients/glossary/art.asp?ArticleKey=1968
Ehlers-Danlos Syndrome, Philadelphia Chapter
ehlersdanlos syndrome Philadelphia Chapter, The Philadelphia basedehlers-danlos syndrome, Philadelphia Chapter goal is to offer
http://hometown.aol.com/daddio5600/myhomepage/profile.html

Extractions: htmlAdWH('7008053', '120', '30'); htmlAdWH('7009912', '234', '60'); Main Create Edit Help Ehlers-Danlos Syndrome Philadelphia Chapter The Philadelphia based Ehlers-Danlos Syndrome, Philadelphia Chapter goal is to offer its members and non-members the emotional support,educational materials and to serve as a vital link to the various communities in the City of Philadelphia.
Ehlers-Danlos Syndrome
ehlersdanlos syndrome. IN THE REST OF THE WORLD. The pictures. Ehlers-DanlosUK Support Group. ehlers-danlos syndrome - Vanderbilt Univ. (US).
http://www.eadv.org/skinweb/ehl-dan.html
R A V E N X::.....: Ehlers-Danlos Syndrome :
ehlersdanlos syndrome CEDA The Canadian Ehlers-Danlos Association. Ehlers-DanlosSyndrome UK Support Group. EDS News Items. Update Hypermobility syndrome.
http://ravenx.editthispage.com/eds

Extractions: Synonyms, Key Words, and Related Terms: EDS, connective tissue disorders, joint laxity, articular hypermobility, skin laxity, hyperextensible skin, abnormal wound healing, hypermobility syndrome, collagen abnormalities, lysyl hydroxylase deficiency, periodontitis, fibronectin, platelet aggregation defect, acrogeria, tissue fragility, vascular rupture, colonic perforation, excessive bruising, easy bruising, prominent venous plexus, petechiae, retinal detachment, dystrophic scarring eMedicine Journal's Pediatric EDS page EDNF: The Ehlers-Danlos National Foundation CEDA: The Canadian Ehlers-Danlos Association Ehlers-Danlos Syndrome UK Support Group ... Update Hypermobility syndrome DISCUSS
Ehlers-Danlos Syndrome
ehlersdanlos syndrome. Paul D. Sponseller, MD. ehlers-danlos syndrome type VIIClincal features and molecular defects. J Bone Joint Surg. 1999; 81A225-239.
http://ortho.hyperguides.com/Tutorials/pediatric_ort/ehlers_danlos/tutorial.asp

Extractions: Ehlers-Danlos syndrome (EDS) is a family of disorders caused by a variety of defects in collagen metabolism ( Slide 1 ). The cardinal feature, common through all subtypes of this syndrome, is hyperelasticity of the skin. In addition to hyperextensibility of skin, joint hypermobility, easy bruisability, soft tissue and bony fragility, calcification of soft tissues, and varying degrees of osteopenia are also present. Diagnosis is primarily clinical and at least 10 types of EDS have been described. The more common forms are summarized in Table 1. Table 1 Slide 1 Abbreviations: AD=autosomal dominant and AR=autosomal recessive. Another classification system has been proposed recently by Beighton et al. This classification simplifies the condition into 6 categories: Classic type . This includes EDS types I and II. It is characterized by hyperextensibility of the skin, tissue fragility, and joint hypermobility. Biochemical studies have revealed defects in type V collagen although locus heterogeneity is present.
Ehlers-Danlos Syndrome
ehlersdanlos syndrome. Inheritance, autosomal dominant. Occurrence, Aftersome discussion allow students to research ehlers-danlos syndrome. There
http://www.usoe.k12.ut.us/curr/Science/core/bio/genetics/ehlers_danlos.htm

Extractions: Ehlers-Danlos Syndrome Inheritance autosomal dominant Occurrence 1 in 5,000 to 1 in 10,000 Description Ehlers-Danlos is a group of connective tissue disorders characterized by articular hypermobility (the ability to flex joints beyond the "normal" range), skin hyperelasticity (the ability to stretch the skin away from the body), and fragile skin and tissues (easy bruising and easily ruptured skin and blood vessels). Diagnosis through a physician familiar with EDS Cause mutations in the genes for collagen Each Protein's Role is Important Background: This disorder is very similar to Marfan Syndrome, and may be introduced in conjunction with one another. As students study the layers of the skin (epidermis and dermis) and joints, some attention should be paid to the role of collagen. Collagen is a protein which provides strength and elasticity and is very important. Activity: Have students research in groups, the role of collagen in the body. Once they understand its importance have them hypothesize what the effects would be on an individual whose collagen did not function properly. After some discussion allow students to research Ehlers-Danlos Syndrome. There are many resources available on the Internet. Once they have learned what really happens to individuals with faulty collagen have them compare their hypotheses to the conclusions. Did anyone predict fragile skin? What about hyper flexible joints? Can your class now understand how important the role is of every protein in the body?

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