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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 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 e-mail or write to the address below. For $10.00 NZ you will receive a copy of Loosely Speaking, the Foundation's newsletter, three times a year.

22. GeneReviews: Ehlers-Danlos Syndrome, Kyphoscoliotic Form
    Your browser does not support HTML frames so you must view ehlersdanlos syndrome, Kyphoscoliotic Form in a slightly less readable form.  
    http://www.geneclinics.org/profiles/eds6/

23. Ehlers-Danlos Syndrome, Kyphoscoliotic Form
    ehlersdanlos syndrome, Kyphoscoliotic Form. ED. Molecular Genetics of ehlers-danlos syndrome, Kyphoscoliotic Form. Gene Symbol. Chromosomal Locus. Protein Name.  
    http://www.geneclinics.org/profiles/eds6/details.html
    
    Extractions: 12 March 2003 Disease characteristics. Ehlers-Danlos syndrome (EDS), kyphoscoliotic form (previously known as EDS VI) is a generalized connective tissue disorder characterized by kyphoscoliosis, joint laxity, muscle hypotonia, and, in some patients, ocular problems. Intelligence is normal; lifespan may be normal, but affected individuals are at risk for rupture of medium-sized arteries and respiratory compromise if kyphoscoliosis is severe. Diagnosis/testing. EDS, kyphoscoliotic form is caused by deficient activity of the enzyme procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 (lysyl hydroxylase). The diagnosis of EDS, kyphoscoliotic form relies upon the demonstration of an increased ratio of deoxypyridinoline to pyridinoline crosslinks in urine measured by HPLC, a highly sensitive and specific test. Molecular genetic testing of the PLOD gene (chromosomal locus 1p36.3-p36.2) that encodes the enzyme lysyl hydroxylase is available on a research basis only.

24. Dermatlas: Online Dermatology Image Library Dermatology Image,Ehlers-Danlos Synd
    Next Result Set. Dermatlas ehlers-danlos syndrome © 2001-04, Dermatlas, Image Name ehlers_danlos_syndrome_em_1_040502, File Type jpg.  
    http://dermatlas.med.jhmi.edu/derm/result.cfm?Diagnosis=-903490152

25. Ehlers-Danlos Syndrome (EDS)
    If your question is not answered here, please contact one of our information specialists. ehlersdanlos syndrome (EDS).  
    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.

26. Ehlers-Danlos Syndrome / Family Village
    ehlersdanlos syndrome. It desires to inspire and support research in the field of connective tissue disorders specifically ehlers-danlos syndrome.  
    http://www.familyvillage.wisc.edu/lib_e-ds.htm
    
    Extractions: Website: http://www.ednf.org/ This organization seeks to provide emotional support and updated information to those affected by Ehlers-Danlos syndrome and to their family members. In addition, EDNF serves as a vital information link to and from the medical community. It desires to inspire and support research in the field of connective tissue disorders specifically Ehlers-Danlos syndrome. The Foundation publishes a quarterly newsletter, Loose Connections, which provides current information on medical advances in EDS, as well as a means to share in the everyday experiences of living with EDS. In addition, a computerized database is maintained which allows interested members to communicate with one another. Local Branches and support groups are forming throughout the U.S. These local branches enable members to meet and network with others affected by EDS, thus decreasing the feeling of isolation so many of us know all so well. Learning conferences are held in various locations throughout the country in an effort to allow patients, family members and medical professionals the opportunity to share information about EDS. Ehlers Danlos Support Club

27. The Ehlers Danlos Syndrome
    The Ehlers Danlos syndrome. Although ehlersdanlos syndrome was once considered to be a fairly rare condition now it is believed to affect 1 in 5,000 people.  
    http://ok.essortment.com/ehlersdanlossy_rgkq.htm
    
    Extractions: The Ehlers Danlos syndrome Once thought to be a rare condition of the connective tissue the Ehlers Danlos Syndrome is now believed to affect 1 in every 5,000 people. The Ehlers-Danlos Syndrome (EDS) is a group of genetic conditions that have resulted from defects in a collagen molecule which would normally give strength and adhesion to the body's tissues. In many cases the disorder affects the skin and it can become excessively extendible (stretchy), fragile and bruise easily. The joints are often affected with or without skin problems. The ligaments and tendons become extremely lax and this can often result in dislocations and the onset of early degenerative osteoarthritis. Also, the walls of the blood vessels, intestines, uterus and also the foetal membranes may be markedly fragile which can often have severe repercussions. The healing of both accidental and surgical wounds is frequently very poor leaving dramatic scarring. Other problems often include prolapse of the heart's mitral valve, aneurysms, hernias, and a range of orthopaedic and dental problems. The manner in which it affects patients in degree of severity is extremely unpredictable. Although Ehlers-Danlos Syndrome was once considered to be a fairly rare condition now it is believed to affect 1 in 5,000 people. It affects both men and women with no predisposition to race or ethnicity. bodyOffer(28912) The condition was named after the two doctors who first grouped the symptoms. Edvard Ehlers was a Danish physician specializing in dermatology and Henri-Alexandre Danlos was a doctor at the Hospital Tenon, Paris, France. Although it wasn't until 1936 that Frederich Parkes-Weber proposed that the name "Ehlers-Danlos Syndrome" be applied to the disorder the condition was well known before then. A Spanish sailor known as George Albes was infamous for being able to stretch the skin on his chest out to arm's length. He was even asked to attend a meeting of physicians at the Academy of Leyden to demonstrate his unusual ability.

28. THE MERCK MANUALSECOND HOME EDITION, Ehlers-Danlos Syndrome In
    ehlersdanlos syndrome. ehlers-danlos syndrome is caused by an abnormality in one of the genes that controls the production of connective tissue.  
    http://www.merck.com/mrkshared/mmanual_home2/sec23/ch279/ch279b.jsp

29. Ehlers-Danlos Syndrome - Information / Diagnosis / Treatment / Prevention
    home musculoskeletal disorders connective tissue ehlersdanlos syndrome ehlers-danlos syndrome. Information • Diagnosis • Treatment • Prevention.  
    http://www.healthcyclopedia.com/musculoskeletal-disorders/connective-tissue/ehle

30. Ehlers-Danlos Syndrome (3)
    Loyola University Medical Education Network, ehlersdanlos syndrome (3). ehlers-danlos syndrome, marked hyperextensibility of the shoulders. non-frame version.  
    http://www.meddean.luc.edu/lumen/MedEd/medicine/dermatology/melton/eds3.htm

31. Ehlers-Danlos Syndrome (1)
    ehlersdanlos syndrome (1). Hyperextensibility of the MCP, PIP, and DIP joints seen in ehlers-danlos syndrome. non-frame version.  
    http://www.meddean.luc.edu/lumen/MedEd/medicine/dermatology/melton/eds1.htm

32. Ehlers-Danlos Syndrome
    ehlersdanlos syndrome. Pathology. ehlers-danlos syndrome (EDS) is a 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.

33. Introduction: Ehlers-Danlos Syndrome - WrongDiagnosis.com
    Introduction ehlersdanlos syndrome. ehlers-danlos syndrome A group of about 10 related inherited connective tissue diseases. Ehlers  
    http://www.wrongdiagnosis.com/e/ehlers_danlos_syndrome/intro.htm

34. Ehlers-Danlos Syndrome - Genetics Home Reference
    ehlersdanlos syndrome. What is ehlers-danlos syndrome? ehlers-danlos syndrome How common is ehlers-danlos syndrome? The overall prevalence  
    http://ghr.nlm.nih.gov/condition=ehlersdanlossyndrome
    
    Extractions: A service of the U.S. National Library of Medicine Home Search Conditions Genes ... Help Ehlers-Danlos syndrome Ehlers-Danlos syndrome is a group of disorders that affect connective tissue (the type of tissue that provides support to 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 factors cause 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. The features of Ehlers-Danlos syndrome vary among the types. All types affect the joints and many also cause skin symptoms and signs. An unusually large range of joint movement, called hypermobility, is characteristic of several forms of Ehlers-Danlos syndrome, particularly the hypermobility type. Joints are unstable and prone to dislocation, chronic pain, and early-onset arthritis. Many people with Ehlers-Danlos syndrome also have soft, velvety skin that is highly elastic (stretchy) and fragile.

35. Ehlers-Danlos Syndrome, Classical Type - Genetics Home Reference
    ehlersdanlos syndrome, classical type. What is ehlers-danlos syndrome, classical type? How common is ehlers-danlos syndrome, classical type?  
    http://ghr.nlm.nih.gov/condition=ehlersdanlossyndromeclassicaltype
    
    Extractions: A service of the U.S. National Library of Medicine Home Search Conditions Genes ... Help Ehlers-Danlos syndrome, classical type 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 classical type is characterized by highly elastic, soft, and doughy skin; unusual scarring; and loose joints. This type of Ehlers-Danlos syndrome combines the types formerly called I and II. Ehlers-Danlos syndrome, classical type is a subtype of Ehlers-Danlos syndrome People with the disorder have smooth, velvety skin that is stretchy, fragile, and easily bruised. Wounds often split open with little bleeding, heal slowly, and leave characteristic thin, wide scars ("cigarette paper" scars). People with this condition also have loose joints with an unusually large range of movement (hypermobility). As a result, joints are prone to dislocation, sprains, and early-onset arthritis. Noncancerous fibrous growths on pressure points (such as elbows) and fatty growths on the forearms and shins are also common.

36. Www.mc.vanderbilt.edu/peds/pidl/genetic/ehlers.html
    ehlersdanlos syndrome Are Genes the Only Cause?ehlers-danlos syndrome Is Diet A Treatment? Contents ehlers-danlos syndrome Environmental and Genetic Factors in EDS and Related Connective Tissue Disorders.  
    http://www.mc.vanderbilt.edu/peds/pidl/genetic/ehlers.html

37. Ehlers-Danlos Syndrome: Diet Considerations
    ehlersdanlos syndrome Diet Changes I Found Helpful. Part I. Also see ehlers-danlos syndrome Diet Changes - Part II. Read my disclaimer and terms of use.  
    http://www.ctds.info/ehlers_danlos_diet.html
    
    Extractions: Con nective Tissue Disorder Home Search Site Map ... Links Also see Ehlers-Danlos Syndrome Diet Changes - Part II Read my Contents: Overview - What My Basic Problems Have Been I've been working with a nutrition oriented doctors and a nutritionist this last year or so, and I must say I've learned more about what's really been wrong with me in the last couple of years than I did in the previous four decades of my life. I was helpful to finally get diagnosed with Ehlers-Danlos syndrome because it provided a rational link for all of my diverse symptoms, but the diagnosis itself didn't help me to improve my health since EDS is considered by most doctors to be an inherited genetic disorder with no known cure. Bit by bit, I've been assembling pieces of information about my health problems, researching nutrition and lately everything has been starting to all fit together and make sense.

38. Ehlers Danlos Syndrome
    Ehlers Danlos Syndrome. Causes. Most forms of ehlersdanlos syndrome (EDS) are transmitted as an autosomal dominant or autosomal recessive trait.  
    http://hw.healthdialog.com/kbase/nord/nord240.htm
    
    Extractions: It is possible that the main title of the report 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. 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

39. Ehlers Danlos, Syndrome : Sites Et Documents Francophones
    Translate this page Ehlers Danlos, syndrome. Menu général CISMeF. Arborescence(s) du thesaurus MeSH contenant le mot-clé Ehlers Danlos, syndrome ehlers-danlos syndrome  
    http://www.chu-rouen.fr/ssf/pathol/ehlersdanlossyndrome.html
    
    Extractions: Ehlers Danlos, syndrome Menu général CISMeF Définition [MeSH Scope Note ; traduction CISMeF] : Groupe hétérogène de maladies héhéditaires du collagène. Les manifestations les plus communes du syndrome d'Ehlers-Danlos sont une peau et des liens hyperextensibles, une fragilité de la peau et une cicatrisation difficile des blessures. appareil cardiovasculaire, maladies hémopathies et maladies lymphatiques maladies et malformations congénitales, héréditaires et néonatales maladies peau et tissu conjonctif Position du mot-clé dans l' (les) arborescence(s) : Vous pouvez consulter Ou consulter ci-dessous une sélection des principales ressources :

40. Kathy Seslar - Ehlers-Danlos Syndrome
    ehlersdanlos syndrome (EDS) is a heterogeneous group of heritable connective tissue disorders, characterized by articular (joint) hypermobility, skin  
    http://www.leaderpro.com/eds/
    
    Extractions: Hi, my name is Kathy Seslar of Tomahawk, Wisconsin, and I have EDS Vascular Type (Ehlers-Danlos Syndrome). I am 43 years old, a wife and mother of two. In the spring of 1998 I realized a life long goal, I received my college degree in elementary education. In the 13 years prior to receiving my degree I was employed and I also did my practice teaching in the Tomahawk (WI) School District. Presently I am teaching special education in the Tomahawk District. I believe God hand picked this job for me because who better to teach children with special needs than a person with special needs herself. Ehlers Danlos Syndrome is a heterogeneous group of heritable connective tissue disorders, characterized by articular (joint) hypermobility, skin extensibility and tissue fragility. There are six major types of EDS. The different types of EDS are classified according to their manifestations of signs and symptoms. Each type of EDS is a distinct disorder that "runs true" in a family. This means that an individual with Vascular Type EDS will not have a child with Classical Type EDS. Individuals with EDS have a defect in their connective tissue, the tissue which provides support to many body parts such as the skin, muscles and ligaments. The fragile skin and unstable joints found in EDS are the result of faulty collagen. Collagen is a protein which acts as a "glue" in the body adding strength and elasticity to connective tissue.

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