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Ehlers-danlos Syndrome:     more books (33)

Diseases Involving the Fasciae: Rheumatoid Arthritis, Systemic Scleroderma, Marfan Syndrome, Hernia, Peritonitis, Scar, Ehlers-Danlos Syndrome Ehlers-Danlos Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-15 Ehlers-Danlos Syndrome Ehlers - Danlos Syndrome - A Medical DictionaryBibliographyand Annotated Research Guide to Internet References - 2004 publication by ICONHealthPublications, 2004 Gale Encyclopedia of Medicine: Ehlers-Danlos syndrome by Java O. Solis MS, 2002-01-01 Ehlers-Danlos syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Java, MS Solis, 2005 Ehlers-Danlos Syndrome: An entry from Gale's <i>Gale Encyclopedia of Medicine, 3rd ed.</i> by Java, MS Solis, 2006 Learning to Be Different: Childs Introduction to Ehlers-Danlos Syndrome by Valerie Armstrong, 1996-05-01 Ehlers-Danlos Syndrome: A Guide for Teachers by Joan Benham, 1995-09-01 Ehlers-Danlos Syndrome by A.P. Barabas, 1995-09-01 Management of Ehlers-Danlos Syndrome by Howard Bird, 2008-07-27 The Ehlers-Danlos syndrome by Peter Beighton, 1970 Pregnancy and Childbirth in Ehlers-Danlos Syndrome by Dodo Merrild, 1995-09-01 Ehlers-Danlos Syndrome: Medical and Practical Information

lists with details

21. The Ehlers Danlos Foundation Of New Zealand
    Support for sufferers of the ehlersdanlos syndrome and related Hypermobility Syndrome and provides some information for the medical profession and  
    http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

22. EMedicine - Ehlers-Danlos Syndrome : Article By G Bradley Schaefer, MD
    ehlersdanlos syndrome - Heritable disorders of connective tissues can be distinguished easily by a phenotype that is characterized by aberrant functioning  
    http://www.emedicine.com/ped/topic654.htm
    
    Extractions: (advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Pediatrics Genetics And Metabolic Disease Last Updated: March 13, 2002 Rate this Article Email to a Colleague Synonyms and related keywords: 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 Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography

23. Philadelphia, PA., Internet Support For Invisible/Hidden Disabilities
    Local Philadelphia, PA support for EDS and connective tissue disorders, also offers a Service Guide for Invisible/Hidden Disabilities.  
    http://hometown.aol.com/daddio5600/
    
    Extractions: The Philadelphia, PA., Internet Support Group For Invisible/Hidden Disabilities was formed in the early parts of September 2000 soon after receiving my DX for Ehlers-Danlos Syndrome (Hypermobility) in August 1999. Before the group stated to produce and publish the "Service Guides for Invisible/Hidden Disabilities" we offered assistance to others who suffered from various conditions, specifically Ehlers-Danlos Syndrome via the internet/support groups and message boards. The groups goal is to offer all who visit this page to gain further insight into what is called an Invisible/Hidden Disability, and to further educate our City, State, Federal Officials and members of the Medical Community to better understand us, our needs and how each group can further assist us in our daily lives as proactive and productive members of society despite our various limitations. Service Guide For Invisible/Hidden Disabilities

24. Danny, 8, To Be Special At Grand Prix The San Diego Union-Tribune
    His condition, ehlersdanlos syndrome, can weaken the vascular system, skin, internal organs and joints.  
    http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

25. Ehlers-Danlos Syndrome - Arthritis And Arthritic Conditions, Medications, And Tr
    Explains arthritis conditions includes symptoms, causes, medications, and treatment. Written and reviewed by a Rheumatologist.  
    http://www.medicinenet.com/ehlers-danlos_syndrome/article.htm
    
    Extractions: Printer-Friendly Format FREE Newsletters Email to a Friend ... Next What is Ehlers-Danlos syndrome? Ehlers-Danlos syndromes is a group of disorders which share common features including easy bruising, joint hypermobility (loose joints), skin that stretches easily (skin hyperelasticity or laxity), and weakness of tissues. The Ehlers-Danlos syndromes are inherited in the genes that are passed from parents to offspring. They are categorized according to the form of genetic transmission into different types with many features differing between patients in any given type. The fragile skin and loose joints is often a result of abnormal genes that produce abnormal proteins that form an inherited frailty of collagen (the normal protein "glue" of our tissues). In 2001, researchers discovered a new form of Ehlers-Danlos syndrome that is caused by an inherited abnormality in a protein other than collagen that also normally plays a role in binding together the cells of our tissues (including the skin, tendons, muscle, and blood vessels). Abnormalities in this protein, called tenascin, also lead to a form of Ehlers-Danlos syndrome. Researchers suspect that tenascin could play a role in regulating the normal distribution of collagen in the connective tissues of the body.

26. The Canadian Ehlers Danlos Association
    Through an educational and informational support network, CEDA is committed to the enhancement of the lives of all persons affected by EhlersDanlos  
    http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

27. Arthritis And Arthritic Conditions, Medications, And Treatment On MedicineNet.co
    Explains arthritis conditions includes symptoms, causes, medications, and treatment. Written and reviewed by a Rheumatologist.  
    http://www.medicinenet.com/ehlers-danlos_syndrome/

28. Ehlers-Danlos Syndrome (EDS)
    Symptoms, diagnosis and treatment of the condition.  
    http://www.arthritis.org/conditions/diseasecenter/eds.asp
    
    Extractions: Resources and Suggestions What Is It? Ehlers-Danlos Syndrome (A-lerz-DAN-los SIN-drome) describes a group of hereditary disorders which mainly affect the skin and joints, but may affect other organs. EDS affects the connective tissues the tissues that support various parts of the body such as skin, muscles, tendons and ligaments. In EDS, the fibrous protein collagen is faulty, causing the connective tissue to not be elastic or strong. What Are the Symptoms? There are 9 types of EDS and symptoms differ depending on the type of EDS. Type I and III have the following: Skin problems, include fragile skin that bruises or tears; soft skin, and slow-healing wounds. Joint problems, including loose, unstable joints; "double-jointed" or overextension of the joints; arthritis-like problems.

29. Arthritis And Arthritic Conditions, Medications, And Treatment On MedicineNet.co
    Doctorproduced information on the different types of EDS, including Tenascin-X Deficiency; treatments, pregnancy considerations, and more.  
    http://www.medicinenet.com/ehlers-danlos_syndrome/index.htm

30. About - Ehlers-Danlos Syndrome.
    ehlersdanlos syndrome. University of Washington, Seattle ehlers-danlos syndrome (EDS) is a group of hereditary disorders that affects mainly the skin  
    http://www.orthop.washington.edu/uw/ehlersdanlos/tabID__3376/ItemID__32/Articles
    
    Extractions: Home Site Map Contact Us Links ... All Articles Ehlers-Danlos Syndrome. University of Washington, Seattle Last updated Friday, February 18, 2005 Basics of ehlers-danlos syndrome Ehlers-Danlos syndrome (EDS) is a group of hereditary disorders that affects mainly the skin and joints, but other organs as well. EDS results in weakness and/or excessive flexibility of the connective tissues of the body. People with EDS are born without the ability to make certain components of the normal connective tissue of the body.

31. Introduction: Ehlers-Danlos Syndrome - WrongDiagnosis.com
    Introduction to ehlersdanlos syndrome as a medical condition including symptoms, diagnosis, misdiagnosis, treatment, prevention, and prognosis.  
    http://www.wrongdiagnosis.com/e/ehlers_danlos_syndrome/intro.htm
    
    Extractions: Ehlers-Danlos syndrome: The problems present in Ehlers-Danlos syndrome (EDS), a group of approximately 10 disorders, include changes in the physical properties of skin, joints, blood vessels, and other tissues such as ligaments and tendons. Researching symptoms of Ehlers-Danlos syndrome: Further information about the symptoms of Ehlers-Danlos syndrome is available including a list of symptoms of Ehlers-Danlos syndrome , other diseases that might have similar symptoms in differential diagnosis of Ehlers-Danlos syndrome , or alternatively return to research other symptoms in the symptom center Misdiagnosis and Ehlers-Danlos syndrome: Research more detailed information about misdiagnosis of Ehlers-Danlos syndrome failure to diagnose Ehlers-Danlos syndrome , or research

32. Symptoms Of Ehlers-Danlos Syndrome - WrongDiagnosis.com
    Symptoms of ehlersdanlos syndrome including signs, symptoms, incubation period, duration, and correct diagnosis.  
    http://www.wrongdiagnosis.com/e/ehlers_danlos_syndrome/symptoms.htm
    
    Extractions: Feedback General information about symptoms of Ehlers-Danlos syndrome: The symptom information on this page attempts to provide a list of some possible symptoms of Ehlers-Danlos syndrome. This symptom information has been gathered from various sources, may not be fully accurate, and may not be the full list of symptoms of Ehlers-Danlos syndrome. Furthermore, symptoms of Ehlers-Danlos syndrome may vary on an individual basis for each patient. Only your doctor can provide adequate diagnosis of symptoms and whether they are indeed symptoms of Ehlers-Danlos syndrome. List of symptoms of Ehlers-Danlos syndrome: The list of symptoms mentioned in various sources for Ehlers-Danlos syndrome includes: Symptoms of Ehlers-Danlos syndrome:

33. .:: Ehlers-Danlos Syndrome, National Association - Sweden ::.
    The purpose of the association is to support members, to inform them and their families, physicians, dentists, other nursing staff and the general public about EDS concerning symptoms and consequences. Find contact details and links.  
    http://www.ehlers-danlos.se/indexEng.html
    
    Extractions: Ehlers-Danlos Syndrome National Association, Sweden. The purpose of the Swedish Ehlers-Danlos Syndrome (EDS) National Association is to support members, to inform them and their families, physicians, dentists, other nursing staff and the general public about Ehlers-Danlos Syndrome concerning symptoms and consequences. If you are viewing this text, your browser lacks the ability to read frames. Don't worry, you can still enjoy our site. All the pages can be viewed from the menu page. Please come inside! Menu Updated March 02, 2005.

34. Ehlers-Danlos Syndrome - Genetics Home Reference
    Where can I find additional information about ehlersdanlos syndrome? What other names do people use for ehlers-danlos syndrome?  
    http://ghr.nlm.nih.gov/condition=ehlersdanlossyndrome
    
    Extractions: Home What's New Browse Handbook ... Search Ehlers-Danlos syndrome On this page: Ehlers-Danlos syndrome is a group of disorders that affect connective tissue, the tissue that supports skin, bones, tendons, ligaments, blood vessels, and other organs. Defects in connective tissue cause the signs and symptoms of Ehlers-Danlos syndrome, which vary from mildly loose joints to life-threatening complications. Genetic changes are related to the following types of Ehlers-Danlos syndrome. In the past, there were more than 10 recognized types of Ehlers-Danlos syndrome. In 1997, researchers proposed a simpler classification that reduced the number of major types to six and gave them descriptive names. These six major types are listed above. Other types of the condition may exist, but they have been reported only in single families or are not well characterized.

35. Ehlers-Danlos Syndrome, Arthrochalasia Type - Genetics Home Reference
    Where can I find additional information about ehlersdanlos syndrome, arthrochalasia type? What other names do people use for ehlers-danlos syndrome,  
    http://ghr.nlm.nih.gov/condition=ehlersdanlossyndromearthrochalasiatype
    
    Extractions: Home What's New Browse Handbook ... Search Ehlers-Danlos syndrome, arthrochalasia type On this page: Ehlers-Danlos syndrome is a group of inherited disorders that affect connective tissue, the tissue that binds and supports the body's muscles, ligaments, organs, and skin. The arthrochalasia type is characterized by very loose joints and dislocations involving both hips. This type of Ehlers-Danlos syndrome combines the types formerly called VIIA and VIIB. Ehlers-Danlos syndrome, arthrochalasia type is a subtype of

36. The Ehlers Danlos Foundation Of New Zealand
    Support for sufferers of the ehlersdanlos syndrome and related Hypermobility Syndrome and provides some information for the medical profession and general public.  
    http://www.edfnz.org.nz
    
    Extractions: The Ehlers Danlos Foundation of New Zealand began as a support group in May 1995 when it was believed there were only twelve families in the country with the condition. Of course this proved a remarkable underestimation of the number of people within New Zealand who actually have EDS. Also catering for people with Hypermobility Syndrome the group achieved charitable status in early 2000. The aim of the organization is to provide emotional support for sufferers of the Ehlers-Danlos Syndrome and HMS, their spouses and family members. Also to create awareness of these conditions by the distribution of information amongst the medical profession and general public. Therefore a newsletter "Loosely Speaking" is published three times a year. It contains both medical information on EDS and personal stories written by the members of the EDFNZ. Individuals with Ehlers-Danlos Syndrome can be affected differently with a variation in the severity and range of symptoms. Because they so often look "normal" it is often difficult to have the condition taken seriously by the medical profession and even within their circle of family and friends. Therefore it can also be an isolating condition and the general lack of awareness and understanding can lead to feelings of frustration, stress and depression. If you're interested in either making a donation or in joining the EDFNZ as a member or Friend of the Foundation please feel free to print out the

37. Ehlers-Danlos Syndrome
    a CHORUS notecard document about ehlersdanlos syndrome.  
    http://chorus.rad.mcw.edu/doc/00134.html

38. Ehlers-Danlos Syndrome
    ehlersdanlos syndrome. autosomal dominant; connective-tissue disorder. hyperelasticity of skin, poor wound healing; hyperextensibility of joints  
    http://chorus.rad.mcw.edu/to-go/00134.html

39. GeneReviews: Ehlers-Danlos Syndrome, Vascular Type
    Your browser does not support HTML frames so you must view ehlersdanlos syndrome, Vascular Type in a slightly less readable form.  
    http://www.genetests.org/query?dz=eds4

40. GeneReviews: Ehlers-Danlos Syndrome, Classic Type
    Your browser does not support HTML frames so you must view ehlersdanlos syndrome, Classic Type in a slightly less readable form. Please follow this link to  
    http://www.genetests.org/query?dz=eds

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