81. Ehlers-Danlos Syndrome The New Health Directory, Directory, Home Health Conditions and Diseases Musculoskeletal Disorders Connective Tissue ehlersdanlos syndrome (12) See Also http://www.thenewhealthfind.com/Health/ConditionsandDiseases/MusculoskeletalDiso

Directory Home Health Conditions and Diseases Musculoskeletal Disorders ... Connective Tissue : Ehlers-Danlos Syndrome (12) See Also: Health: Conditions and Diseases: Musculoskeletal Disorders: Connective Tissue: Fibromyalgia Health: Conditions and Diseases: Musculoskeletal Disorders: Connective Tissue: Hypermobility Syndrome Health: Conditions and Diseases: Musculoskeletal Disorders: Connective Tissue: Marfan Syndrome Ehlers-Danlos National Foundation - Provides support and information to those affected by Ehlers-Danlos syndrome and their families. Canadian Ehlers-Danlos Association - Working together to provide assistance, support and resources for people living with this rare genetic disorder. Arlene Brandeis' Intuitive Art - An expression of the loss of family members to genetic anomalies including Ehlers-Danlos Syndrome, Acute Intermittent Porphyria, and Hypolipoproteinemia. Information provided about each. Damaged - A Journal - The personal diary of a young woman learning to live with Ehlers Danlos Syndrome. Ehlers-Danlos Hope - Personal plea for help from a sufferer in Syria.

82. NEJM -- A Recessive Form Of The Ehlers-Danlos Syndrome Caused By Tenascin-X Defi Next Next. A Recessive Form of the Ehlers–Danlos Syndrome Caused by TenascinX Deficiency. ehlers-danlos syndromeMolecular Genetics Beyond the Collagens. http://content.nejm.org/cgi/content/short/345/16/1167

HOME SEARCH CURRENT ISSUE PAST ISSUES ... HELP Please sign in for full text and personal services Previous Volume 345:1167-1175 October 18, 2001 Number 16 Next Joost Schalkwijk, Ph.D., Manon C. Zweers, Ph.D., Peter M. Steijlen, M.D., Willow B. Dean, B.A., Glen Taylor, B.A., Ivonne M. van Vlijmen, M.Sc., Brigitte van Haren, M.D., Walter L. Miller, M.D., and James Bristow, M.D. Full Text PDF Editorial by Byers, P. H. ... Chapters at Harrison's ABSTRACT Background disorder caused by defects in fibrillar-collagen metabolism. Mutations in the type V collagen genes account for up to 50 many other cases are unexplained. We investigated whether the deficiency of the tenascins, extracellular-matrix proteins that are highly expressed in connective tissues, was associated with Methods We screened serum samples from 151 patients with the syndrome; 75 patients with psoriasis; 93 patients with rheumatoid arthritis; and 21 healthy persons for the presence of tenascin-X and tenascin-C by enzyme-linked immunosorbent assay. We examined the expression of tenascins and type V collagen in skin by immunohistochemical methods and sequenced the tenascin-X gene.

83. NEJM -- Clinical And Genetic Features Of Ehlers-Danlos Syndrome Type IV, The Vas Clinical and Genetic Features of Ehlers–Danlos Syndrome Type IV, the Vascular Type. Increased Carotid Wall Stress in Vascular ehlersdanlos syndrome. http://content.nejm.org/cgi/content/short/342/10/673

HOME SEARCH CURRENT ISSUE PAST ISSUES ... HELP Please sign in for full text and personal services Volume 342:673-680 March 9, 2000 Number 10 Next A correction has been published: N Engl J Med 2001;344(5):392 Melanie Pepin, M.S., Ulrike Schwarze, M.D., Andrea Superti-Furga, M.D., and Peter H. Byers, M.D. Full Text PDF Editorial by Pyeritz, R. E. ... Chapters at Harrison's ABSTRACT Background type, results from mutations in the gene for type III procollagen ). Affected patients are at risk for arterial, bowel, and uterine rupture, but the timing of these events, their frequency, and the course of the disease are not well documented. Methods We reviewed the clinical and family histories of and medical and surgical complications in 220 index patients with and 199 of their affected relatives. We identified the underlying mutation in 135 index patients. Results Complications were rare in childhood; 25 percent of the index patients had a first complication by the age of 20 years, and more than 80 percent had had at least one complication by the age of 40. The calculated median survival of the entire

84. HealthCentral - Pediatrics Encyclopedia - Ehlers-Danlos Syndrome ehlersdanlos syndrome. Causes, incidence, and risk factors ehlers-danlos syndrome involves abnormal formation of connective tissue. http://www.healthcentral.com/peds/top/001468.cfm

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85. :: Ez2Find :: Ehlers-Danlos Syndrome URL http//michianaednf.org; ehlersdanlos syndrome Information - Site Info - Translate www.orthop.washington.edu/arthritis/types/ehlersdanlos/01; Ehlers http://ez2find.com/cgi-bin/directory/meta/search.pl/Health/Conditions_and_Diseas

Guide : Ehlers-Danlos Syndrome Global Metasearch Any Language English Afrikaans Arabic Bahasa Melayu Belarusian Bulgarian Catala Chinese Simplified Chinese Traditional Cymraeg Czech Dansk Deutsch Eesti Espanol Euskara Faroese Francais Frysk Galego Greek Hebrew Hrvatski Indonesia Islenska Italiano Japanese Korean Latvian Lietuviu Lingua Latina Magyar Netherlands Norsk Polska Portugues Romana Russian Shqip Slovensko Slovensky Srpski Suomi Svenska Thai Turkce Ukrainian Vietnamese Mode All Words Any Word Phrase Results Timeout Depth Adult Filter Add to Favorites Other Search Web News Newsgroups Images Guides Ehlers-Danlos Syndrome ez2Find Home Directory Health Conditions and Diseases ... Connective Tissue : Ehlers-Danlos Syndrome Related Categories Health: Conditions and Diseases: Musculoskeletal Disorders: Connective Tissue: Fibromyalgia Health: Conditions and Diseases: Musculoskeletal Disorders: Connective Tissue: Hypermobility Syndrome Health: Conditions and Diseases: Musculoskeletal Disorders: Connective Tissue: Marfan Syndrome Web Sites Arthritis Foundation Disease Center: Ehlers-Danlos Syndrome [Site Info] [Translate] [Open New Window] While EDS and Arthritis are two separate diseases, there are many characteristics in common. Additionally, EDS patients are at risk of developing OA. In addition to EDS information, site provides valuable pain and life management resources for patients. URL: http://www.arthritis.org/conditions/diseasecenter/eds.asp

86. Short Description Of Cell Lines. Pathology: Ehlers-Danlos Syndrome Version 4.200205, Short description of cell lines. Pathology ehlersdanlos syndrome OMIM Home. - By selecting the cell line name, you http://www.biotech.ist.unige.it/cldb/pat12.html

Version Short description of cell lines. Pathology: Ehlers-Danlos syndrome OMIM Home By selecting the cell line name , you will receive the detailed description of the cell line By selecting one of the terms between parentheses, you will receive the list of all relevant cell lines You can search any term of the list by using the 'Find' utility of your browser FIB-EDII1 human, Caucasian skin, fibroblast DSB ... By Beatrice...

87. Short Description Of Cell Lines. Pathology: Ehlers-Danlos Syndrome, Type III 130 Version 4.200205, Short description of cell lines. Pathology ehlersdanlos syndrome, type III 130020 OMIM record. - By selecting http://www.biotech.ist.unige.it/cldb/pat202.html

Version Short description of cell lines. Pathology: Ehlers-Danlos syndrome, type III OMIM record By selecting the cell line name , you will receive the detailed description of the cell line By selecting one of the terms between parentheses, you will receive the list of all relevant cell lines You can search any term of the list by using the 'Find' utility of your browser EDS 100 human, Caucasian skin, fibroblast BGEBS ... By Beatrice...

88. International Ehlers-Danlos Syndrome Meetup Day International ehlersdanlos syndrome Meetup Day. in 12 Days. WHAT. Meetup with other local sufferers of ehlers-danlos syndrome (EDS). http://eds.meetup.com/

@import url("http://www.meetup.com/style/common.css"); @import url("http://www.meetup.com/style/topic.css"); @import url("http://www.meetup.com/style/hide-from-ie-mac.css"); @import url("http://www.meetup.com/style/images.css"); Your Meetup now has its own Message Boards! Join the conversation! Meetup Home Discuss Meetup.com Sign In ... Ehlers-Danlos Syndrome International Ehlers-Danlos Syndrome Meetup Day in 3 Days WHAT Meetup with other local sufferers of Ehlers-Danlos Syndrome (EDS). Gather and share advice, offer support, and learn more about this connective tissue disorder. WHEN Saturday, June 5 @ 11:00AM (1st Saturday of every month.) WHO EDS Sufferers Worldwide (and friends.) So far, have signed up. AGENDA T.B.D. More info. Next Meetup Members ... Links Join other EDS Sufferers near you! Ehlers-Danlos Syndrome Meetups can happen in up to 646 cities worldwide on the same day. Enter your location to find the one near you: writeForm("horiz") US Residents, enter your 5-digit Zip Code: Non-US Residents, select your

89. AR Online » Case Reports » MRI » Ehlers-Danlos Syndrome (EDS) Type IV ehlersdanlos syndrome (EDS) type IV. By His cardiac examination remained normal. Diagnosis ehlers-danlos syndrome (EDS) type IV. Imaging http://www.appliedradiology.com/case/case.asp?ID=382&SubCatID=191&CatID=29&Threa

90. MUTATION ANALYSIS IN VARIOUS TYPES OF THE EHLERS-DANLOS SYNDROME (EDS) researchproject. MUTATION ANALYSIS IN VARIOUS TYPES OF THE ehlersdanlos syndrome (EDS). The ehlers-danlos syndrome (EDS) is a genetically http://www.research-projects.unizh.ch/med/unit41900/area549/p1900.htm

research project MUTATION ANALYSIS IN VARIOUS TYPES OF THE EHLERS-DANLOS SYNDROME (EDS) The Ehlers-Danlos syndrome (EDS) is a genetically and clinically heterogeneous group of connective tissue disorders which have in common joint hypermobility, skin hyperextensibility and fragility. Variable expression of these features, different modes of inheritance and the presence of distinctive associated manifestations distinguish the 10 types of the syndrome. Mutations in the genes encoding collagen V (COL5A1 and COL5A2) have been identified in several patients/families with the classical form of EDS (MIM 130000) (EDS I and II). We have recently identified the first glycine to glutamic acid substitution (G1489E) in the alpha1(V) collagen chain. Furthermore, increasing evidence indicates that haploinsufficiency of COL5A1 which is caused by mutations leading to non-sense mediated mRNA decay, is a common cause of classical EDS. We intend to determine whether mutations in COL5A1 and COL5A2 are the prevalent cause of classical EDS. The vascular type of EDS (EDS IV, MIM 130050) is caused by mutations in the COL3A1 gene, which lead to impaired secretion and/or instability of structurally abnormal collagen III molecules. The aim of our study is to correlate the clinical course of individuals affected with EDS IV with their biochemical data and genotype. Furthermore, we would like to investigate whether haploinsufficiency of COL3A1, which has only recently been suspected, may cause the severe phenotype or rather a milder variant.

91. »»Ehlers-Danlos-Syndrome Reviews«« EhlersDanlos-Syndrome Reviews. The ehlers-danlos syndrome. Published in Unknown Binding by Heinemann Medical (1970). Author Peter Beighton. Amazon base price $. http://www.health-issue-books.com/Dyspnea/Ehlers-Danlos-Syndrome/

Ehlers-Danlos-Syndrome Reviews Related Subjects: Dyspnea Book reviews for "Ehlers-Danlos-Syndrome" sorted by average review score: The Ehlers-Danlos syndrome Published in Unknown Binding by Heinemann Medical (1970) Author: Peter Beighton Amazon base price: Average review score: No reviews found. Ehlers-Danlos Syndrome: Medical and Practical Information Published in Plastic Comb by SignQuest Publishers (January, 1997) Author: Lindalee Massoud Amazon base price: Average review score: No reviews found. The Official Patient's Sourcebook on Ehlers-Danlos Syndrome: A Revised and Updated Directory for the Internet Age Published in Paperback by Icon grp int (August, 2002) Author: Icon Health Publications Amazon base price: Collectible price: Average review score: No reviews found. Related Subjects: Dyspnea Search for a Health Issue Book Sort by: Rank Last Modified Date Title Path Reverse Sort

92. Hypermobility Forum For People With Marfan, EDS This is a moderated discussion board for Hypermobility syndrome, Marfan, and ehlersdanlos. Includes personal experiences, traditional and alternative treatment, and pain. http://marge.com/hypermobility/

Welcome to Hypermobility Forum for people with Marfan, EDS Your browser does not support Frames. Therefore, navigation of Hypermobility Forum for people with Marfan, EDS will not be aided by having a menu present at all times. The following is the menu made available to those with a frame-compatible browser: Top (Index) Instructions Formatting Troubleshooting ... User Profile Administration (Requires Frames) Click Here to Start

93. Ehlers Danlos Syndrome Ehlers Danlos syndrome Menu. This is a webforum to discuss and comment on Ehlers Danlos syndrome. Click here to Enter a new Neurology WebForum article Click Here to Read our Forum Disclaimer and http://neuro-www.mgh.harvard.edu/forum/EhlersDanlosSyndMenu.html

Ehlers Danlos Syndrome Menu This is a webforum to discuss and comment on Ehlers Danlos Syndrome. Click here to Enter a new Neurology WebForum article... This Web Forum is not moderated in any sense. Anyone on the Internet can post articles or reply to previously posted articles, and they may do so anonymously. Therefore, the opinions and statements made in all articles and replies do not represent the official opinions of MGH and MGH Neurology. Neither is MGH or MGH Neurology responsible for the content of any articles or replies. No messages are screened for content. - Very Important Message! - Please Click Here to Read Current Posts: 8/20/98 to Present Useful Websites can be found and posted here! (1/3/00) 7:20 AM (1/1/00) 3:49 PM (12/30/99) 11:33 PM ... test (8/20/98) 15:41 IMPORTANT: If this page seems to be missing recently added documents, click the "Reload Page" button on your Web Browser to update the menu. Return to the main Neurology WebForum Page. These forums are maintained by the Department of Neurology at Massachusetts General Hospital John Lester - Webspinner

94. Association Française Des Syndromes D'Ehlers-Danlos (AFSED) Informations, soutien et mise en relation des familles. http://assoc.wanadoo.fr/ehlers.danlos/

Bonjour, Le site internet de l'AFSED a changé d'adresse ! Veuillez désormais utiliser l'adresse suivante pour le consulter : http://www.afsed.com

95. Ehlers – Danlos Syndrome Ehlers – danlos syndrome,. Print this article, (Edvard Ehlers, 1863–1937, Danish dermatologist; Henri Alexandre Danlos, 1844–1912. http://www.amershamhealth.com/medcyclopaedia/Volume V 2/EHLERS DANLOS SYNDROME.

Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Ehlers – danlos syndrome, (Edvard Ehlers, 1863–1937, Danish dermatologist; Henri Alexandre Danlos, 1844–1912. French dermatologist), several rare complex abnormalities characterized by hyperelasticity and fragility of the skin and hypermobility of the joints. Cardiovascular abnormalities vary from nonexistent to severe. Mitral valve prolapse is the most frequent abnormality. The severest lesions occur in Ehlers – Danlos type IV with a high frequency of spontaneous rupture of large and medium size arteries especially the aortic arch branches and the abdominal aorta and its branches. Pregnancy is hazardous in women with this syndrome because of a high incidence of arterial rupture. The arterial abnormalities may be demonstrated by X-ray aortography or selective arteriography. Echocardiography is the optimal technique for evaluating mitral valve prolapse and regurgitation. MRI and contrast-enhanced MR angiography can be used for identification and monitoring of aortic and arterial abnormalities associated with these syndromes. CBH The Encyclopaedia of Medical Imaging Volume V:2 Contacts GE Healthcare Making Waves

96. Ehlers Danlos Syndrome Ehlers danlos syndrome,. Print this article, Persistent joint effusion or haemarthrosis may be noted in patients with Ehlers Danlos syndrome. http://www.amershamhealth.com/medcyclopaedia/medical/Volume III 1/EHLERS DANLOS

Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Ehlers danlos syndrome, (Edward Ehlers, 18631937, Danish dermatologist and Henri Alexandre Danlos, 18441912, French dermatologist), the general name for a group of 11 syndromes involving abnormalities of connective tissue characterized by hyperelasticity and fragility of the skin, hyperlaxity of the joints and a bleeding diathesis . Other systems that may be involved are the eye and the gastrointestinal, bronchopulmonary, genitourinary and cardiovascular systems. These syndromes vary genetically and biochemically but share the same complex of clinical abnormalities. Type IV is the most serious form of the disease and carries a decreased life expectancy. The primary disorder is a defect in collagen synthesis. No primary bone abnormality has been identified. Molluscoid fibrous tumours composed of proliferating connective tissue and degenerated fat are found predominantly on the pressure points of the body. Patients also exhibit subcutaneous spherules of necrotic fat in the skin that may be related to subclinical trauma. The bleeding diathesis may result from abnormalities in the vessel walls and defects in the supporting perivascular tissues that cause failure of tamponade. Subcutaneous haematomas are also seen. The joint hypermobility makes it possible for patients to touch the thumb to the forearm, dorsiflex the fifth finger beyond 90, hyperextend the elbow beyond 10, and hyperextend the knee beyond 10 (

97. Ehlers Danlos, Syndrome : Arborescences MeSH Translate this page Ehlers Danlos, syndrome arborescences MeSH. Menu général CISMeF. Vous pouvez aussi consulter toutes les arborescences des mots http://www.chu-rouen.fr/navimesh/E/naviehlersdanlossyndrome.html

Ehlers Danlos, syndrome : arborescences MeSH Menu général CISMeF Vous pouvez aussi consulter toutes les arborescences des mots clés utilisés dans CISMeF appareil cardiovasculaire, maladies vaisseaux, maladies troubles hémorragiques vasculaires angiomatose hémorragique familiale ... xeroderma pigmentosum 07 janvier 2004 courriel Menu général CISMeF Haut de page © CHU de Rouen . Toute utilisation partielle ou totale de ce document doit mentionner la source.

98. Ehlers Danlos Syndrome Ehlers Danlos syndrome Important It is possible that the main title of the report Ehlers Danlos syndrome is not the name you expected. http://my.webmd.com/hw/health_guide_atoz/nord240.asp

var guid_source = ""; var guid_source_id = ""; //unused var encodedurl = ""; WebMD Today Home WebMD News Center Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Quizzes, Calculators Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map You are in Medical Library Choose a Topic Our Content Sources Ask A Question Clinical Trials Health Guide A-Z Health Topics Symptoms Medical Tests Medications ... For a Complete Report Ehlers Danlos Syndrome Important It is possible that the main title of the report Ehlers Danlos Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms E-D Syndrome EDS Disorder Subdivisions EDS Gravis Type (Type 1) Ehlers-Danlos Syndrome Type II EDS Mitis Type (Type II) Ehlers-Danlos Syndrome Type III Benign Hypermobility Syndrome (Type III) Ehlers-Danlos Syndrome Type IV EDS Arterial-Ecchymotic Type (Type IV) Ehlers-Danlos Syndrome Type V Ehlers-Danlos Syndrome Type VI EDS Kyphoscoliotic Type (Type VI) EDS Ocular-Scoliotic Type (Type VI) Ehlers-Danlos Syndrome Type VII, Autosomal Dominant

99. Ehler Danlos Syndrome MEDSTUDENTS-METABOLIC DISORDERS Medstudents Homepage. Ehler Danlos syndrome. Differential diagnosis. Major differential diagnosis is Marfan syndrome and some forms of osteogenese imperfecta. http://www.medstudents.com.br/metdis/metdis7.htm

Metabolic Disorders Medstudents' Homepage Ehler Danlos Syndrome Definition Ehler Danlos syndrome is one of the inheritable connective tissues disorders along with: Marfan syndrome, pseudoxantoma elasticum, osteogenese imperfecta, chondrodysplasias, epidermolysis bullosa and Alport syndrome. It comprises a group of ten different subtypes. The main clinical manifestations are skin fragility, abnormal scar formation, excessive bruising, joint laxity and sometimes rupture of viscera and arteries. Etiology The basic defect is in the synthesis of collagen type I and III, leading to low tensile strength of skin and artery wall. Clinical manifestations Type III, the so called familial hypermobility disease account for the majority of cases observed. Clinical manifestations varies among the ten groups. Type I (Gravis), type II (mitis), type V (X-linked) and type X have similar clinical manifestations, except for the greater gravity of these in type I. They present with marked joint laxity, hyperextensible skin, easy bruising and "cigarette paper scars" in areas of trauma. Major complication are joint dislocation, skin fragility and osteoarthritis of early onset.

100. Ehlers Danlos Syndrome,E-D Syndrome,EDS,EDS Gravis Type,EDS Mitis Type,Ehlers-Da Ehlers Danlos syndrome,ED syndrome,EDS. The GAPS INDEX to Information on the Internet about Genetic Disorders and Birth Defects. Ehlers Danlos syndrome http://www.icomm.ca/geneinfo/eds.htm

For Information on Workshops and Seminars for Special Needs Children click here Ehlers Danlos Syndrome,E-D Syndrome,EDS The GAPS INDEX to Information on the Internet about Genetic Disorders and Birth Defects Genetic Information and Patient Services, Inc. (GAPS) HOME DISORDERS GLOSSARY Ehlers Danlos Syndrome (as defined by the National Organization for Rare Disorders also known as: E-D Syndrome EDS Disorder Subdivisions EDS Gravis Type (Type 1) Ehlers-Danlos Syndrome Type II EDS Mitis Type (Type II) Ehlers-Danlos Syndrome Type III Benign Hypermobility Syndrome (Type III) Ehlers-Danlos Syndrome Type IV EDS Arterial-Ecchymotic Type (Type IV) Ehlers-Danlos Syndrome Type V Ehlers-Danlos Syndrome Type VI EDS Kyphoscoliotic Type (Type VI) EDS Ocular-Scoliotic Type (Type VI) Ehlers-Danlos Syndrome Type VII, Autosomal Dominant EDS Types VIIA and VIIB Arthrochalasis Multiplex Congenita (Type VII) Ehlers-Danlos Syndrome Type VII, Autosomal Recessive EDS Type VIIC Dermatosparaxis (Type VII) Ehlers-Danlos Syndrome Type VIII Ehlers-Danlos Syndrome Type IX (obsolete) Ehlers-Danlos Syndrome Type X EDS Dysfibronectinemic Type (Type X) Ehlers-Danlos Syndrome Type XI (obsolete) EDS Classical Type (formerly EDS I and EDS II) EDS Hypermobility Type (formerly EDS III) EDS Vascular Type (formerly EDS IV) EDS Kyphoscoliosis Type (formerly EDS VI) EDS Arthrochalasia Type (formerly EDS VII, Autosomal Dominant)

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