Home  - Health_Conditions - Ehlers-danlos Syndrome

Books Baby Camera Phones Computers Games DVD Electronics Kitchen Magazines Music Garden Software Tools Toys Video Apparel & Accessories Jewelry & Watches Musical Instruments Health & Personal Care Beauty Sports & Outdoors Office Products

e99.com Bookstore

Images

Newsgroups

61-80 of 103    Back | 1  | 2  | 3  | 4  | 5  | 6  | Next 20

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Ehlers-danlos Syndrome:     more books (33)

Issues and Management of Joint Hypermobility: A Guide for the Ehlers-Danlos Syndrome Hypermobility Type and the Hypermobility Syndrome by Brad T. Tinkle, 2008-09-30 Joint Hypermobility Handbook-A Guide for the Issues & Management of Ehlers-Danlos Syndrome Hypermobility Typeand the Hypermobility Syndrome by Brad T Tinkle, 2010-07-12 The Official Patient's Sourcebook on Ehlers-Danlos Syndrome: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-08 Ehlers-Danlos Syndrome - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-09-28 Ehlers-Danlos syndrome, classical type: case management.(Disease Management): An article from: Dermatology Nursing by Sara E. Whitelaw, 2004-10-01 2009 Conquering Ehlers-Danlos Syndrome (Cutis Elastica) - The Empowered Patient's Complete Reference - Diagnosis, Treatment Options, Prognosis (Two CD-ROM Set) by PM Medical Health News, 2009-04-10 Ehlers-Danlos syndrome 21st Century Ultimate Medical Guide to Ehlers-Danlos Syndrome (Cutis Elastica) - Authoritative, Practical Clinical Information for Physicians and Patients, Treatment Options (Two CD-ROM Set) by PM Medical Health News, 2009-04-10 Ehlers-Danlos Syndrome (Cutis Elastica) Toolkit - Comprehensive Medical Encyclopedia with Treatment Options, Clinical Data, and Practical Information (Two CD-ROM Set) by U.S. Government, 2009-04-10 Name that syndrome: JHS or EDS-HM?(LETTERS)(joint hypermobility syndrome)(Ehlers-Danlos syndrome-hypermobility type)(Letter to the editor): An article from: Internal Medicine News by Gale Reference Team, 2006-08-01 Contortion: Ehlers-Danlos Syndrome, Hypermobility, Whiplash, Joint Dislocation, Frontbend 21st Century Complete Medical Guide to Ehlers-Danlos Syndrome (EDS), Hypermobility, Authoritative Federal Government Clinical Data and Practical Information for Patients and Physicians by PM Medical Health News, 2004-04 Ehlers-Danlos syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Children's Health: Infancy through Adolescence</i> by Judith Sims, Java, M.S. Solis, 2006 Ehlers-Danlos Syndrome - A Medical Dictionary, Bibliographynd Annotated Research Guide to Internet References, 2004 publication by various, 2004-01-01

lists with details

61. Health Library -
    Ehlers Danlos Syndrome. Synonyms. ED Syndrome; EDS. Disorder Subdivisions. EDS Gravis Type (Type 1); ehlersdanlos syndrome Type II; EDS Mitis Type (Type II);  
    http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/topic.asp?hwid=

62. EHLERS-DANLOS SYNDROME
    Terms of Use. ehlersdanlos syndrome. Specialty Definition ehlers-danlos syndrome. Domain, Definition. Health. Top. Specialty Definition ehlers-danlos syndrome.  
    http://www.websters-online-dictionary.org/definition/english/Eh/Ehlers-Danlos Sy
    
    Extractions: Philip M. Parker, INSEAD. EHLERS-DANLOS SYNDROME Specialty Definition: EHLERS-DANLOS SYNDROME Domain Definition A heterogeneous group of inherited collagen diseases. The most common manifestions of Ehlers-Danlos Syndrome are hyperextensible skin and joints, skin fragility and reduced wound healing capability. ( references Hyperelastic and fragile skin, hyperflexible joints, and fragile blood vessels, with resulting hematomata which sometimes develops into pseudotumors. The condition has a hereditary tendency and often affects the skin of the eyelids. Source: European Union. references Source: compiled by the editor from various references ; see credits. Top Specialty Definition: Ehlers-Danlos syndrome (From Wikipedia , the free Encyclopedia) Ehlers-Danlos syndrome is a group of rare genetic disorders that diminish the body's ability to make connective tissues. This results in unstable, flexible joints, including double-jointedness, and elastic, fragile, soft skin that easily forms welts and scars. Other symptoms include eye problems and nearsightedness. Source: compiled by

63. Ehlers-Danlos Syndrome Information Diseases Database
    2 synonyms or equivalents were found. ehlersdanlos syndrome aka/or Cutis hyperelastica Medical information linksehlers-danlos syndrome specific sites.  
    http://www.diseasesdatabase.com/ddb4131.htm

64. Ehlers-Danlos Syndrome (www.whonamedit.com)
    ehlersdanlos syndrome In 1936, Frederick Parkes-Weber suggested that the disturbance should bed named Ehlers–Danlos syndrome.  
    http://www.whonamedit.com/synd.cfm/2017.html
    
    Extractions: This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. Arthrocalasia multiplex congenita, cutis elastica syndrome, cutis hypereleastica, cutis hyperelastica dermatorrhexis, cutis laxa, dermatorrhexis with dermatochalasis and arthrochalasis, dystrophia mesodermalis, dystrophia mesodermalis congenita, cutis hyperelastic dermatorrhexis, elastic skin, fibrodysplasia elastica, fibrodysplasia elsatica generalisata, marfanoides Hypermobilitäts-Syndrom (German), mal de Meleda, rubber man, rubber skin.

65. Disease Directory : Musculoskeletal Disorders : Connective Tissue : Ehlers-Danlo
    Diseases Musculoskeletal Disorders Connective Tissue ehlersdanlos syndrome. AllRefer Health - ehlers-danlos syndrome - ehlers-danlos syndrome. PA.  
    http://www.diseasedirectory.net/Musculoskeletal_Disorders/Connective_Tissue/Ehle
    
    Extractions: Ehlers-Danlos Syndrome ... Connective Tissue : Ehlers-Danlos Syndrome AllRefer Health - Ehlers-Danlos Syndrome - Ehlers-Danlos Syndrome. PA. Review provided by VeriMed Healthcare Network. . Main Page of Ehlers-Danlos Syndrome. ADAM. ADAM, Inc. 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. BEASLEY-COHEN - EHLERS-DANLOS SYNDROME WITH MENTAL RETARDATION - Features Listed For BEASLEY-COHEN - EHLERS-DANLOS SYNDROME WITH MENTAL RETARDATION. McKusick: 225320. Deafness, non-specific; Cataract; Canadian Ehlers-Danlos Association - Working together to provide assistance, support and resources for people living with this rare genetic disorder. Damaged - A Journal - The personal diary of a young woman learning to live with Ehlers Danlos Syndrome. disability - Ehlers-Danlos Syndrome - Ehlers-Danlos Syndrome. Ehlers-Danlos Syndrome From the National Organization for Rare Disorders (NORD); Ehlers-Danlos Syndrome From the University of Washington; EDS Today - The newsletter for, by, and about people with the condition. Includes featured articles, columns, and contact information for support groups worldwide.

66. DermIS / Main Menu / DOIA / Ehlers-Danlos Syndrome / Images
    DermIS / main menu / DOIA / ehlersdanlos syndrome / images, deutsch español portugues français. / images for the diagnosis ehlers-danlos syndrome .  
    http://dermis.multimedica.de/doia/diagnose.asp?zugr=d&lang=e&diagnr=756800&topic

67. DermIS / Main Menu / DOIA / Ehlers-Danlos Syndrome / Info
    // information on the diagnosis ehlersdanlos syndrome . definition. CUTIS ELASTICO, SINDROME DE EHLERS-DANLOS. Do YOU suffer from ehlers-danlos syndrome ?  
    http://dermis.multimedica.de/doia/diagnose.asp?zugr=d&lang=e&diagnr=756800&topic

68. KinderStart - Health/Medical/Dental : Major Diseases/Conditions : Ehlers-Danlos
    Home Health/Medical/Dental Major Diseases/Conditions ehlersdanlos syndrome. Web Pages. The following links are in English EDS  
    http://www.kinderstart.com/healthmedicaldental/majordiseasesconditions/ehlersdan

69. EHLERS-DANLOS SYNDROME : Contact A Family - For Families With Disabled Children:
    printer friendly, ehlersdanlos syndrome, ehlers-danlos syndrome SUPPORT GROUP. ehlers-danlos syndrome Support Group PO Box 335 Farnham  
    http://www.cafamily.org.uk/Direct/e21.html
    
    Extractions: helpful? yes no Ehlers-Danlos: Arthrochalasis-Multiplex Congenita; Cutis Hyperelastica; EDS Ehlers-Danlos syndrome consists of several types of genetic connective tissue disorders. In general, these are due to collagen (a naturally occurring protein) abnormality. Common characteristics include abnormalities of the skin, ligaments and, in some instances, internal organs. Problems include fragile andIor stretchy skin, bruising, poor wound healing and loose joints, which are prone to dislocation and subluxation (partial dislocation). Chronic joint and limb pain is common even when skeletal radiographs are normal. Early degenerative arthritis, mitral valve prolapse and hernias may also present problems. Prematurity due to rupture of the fetal membranes can occur in pregnancy. When bruising presents in a child it may be incorrectly attributed to non-accidental injury. These problems form the major difficulties bringing patients to the notice of Medical and Surgical Specialists. Many patients will be directed to Physiotherapy and Occupational Therapy for help with the musculoskeletal and ergonomic aspects.

70. Musculoskeletal Disorders, Connective Tissue, Ehlers-Danlos Syndrome
    Submit Your Site to the ehlersdanlos syndrome category. Sponsored ehlers-danlos syndrome Sites. Submit Your Site to the ehlers-danlos syndrome category.  
    http://www.iseekhealth.com/ehlers-danlos_syndrome-1884.php

71. Your Health - Ehlers-Danlos Syndrome
    ehlersdanlos syndrome. by Rick Alan. Definition. ehlers-danlos syndrome (EDS) is a group of rare hereditary disorders involving connective tissues.  
    http://www.aurorahealthcare.org/yourhealth/healthgate/getcontent.asp?URLhealthga

72. University Of Miami School Of Medicine - Glossary - Ehlers-Danlos Syndrome
    Diseases and Conditions. ehlersdanlos syndrome. ehlers-danlos syndrome. What is ehlers-danlos syndrome? ehlers-danlos syndromes is  
    http://www.med.miami.edu/patients/glossary/art.asp?ArticleKey=1968

73. Ehlers-Danlos Syndrome
    ehlersdanlos syndrome. by Rick Alan. Definition. ehlers-danlos syndrome (EDS) is a group of rare hereditary disorders involving connective tissues.  
    http://www.somersetmedicalcenter.com/1379.cfm
    
    Extractions: Community Advisor Search Send to a friend Home  Diseases, Conditions and Injuries by Rick Alan Definition Causes Risk Factors ... Organizations Ehlers-Danlos syndrome (EDS) is a group of rare hereditary disorders involving connective tissues. Connective tissues are the tissues that support parts of the body. Examples of connective tissues are skin, tendons, ligaments, and muscles. EDS usually results in over-flexible (hypermobile) joints, over-elastic (hyperelastic) skin, and fragile tissue. EDS is caused by defects in the genes that control the formation of connective tissue. The specific genetic defect in most types of EDS affects the production of collagen. Collagen is a structural protein. It strengthens and provides elasticity to connective tissue. A risk factor is something that increases your chances of getting a disease or condition. Risk factors for EDS include: The severity of EDS symptoms varies from mild to very severe and debilitating. Symptoms depend on the specific type of EDS. The most common symptoms of EDS include: Loose, unstable joints that are very prone to:

74. Ehlers-Danlos Syndrome
    ehlersdanlos syndrome. 01- Goodman, RM – Chronic temporomandibular joint subluxation in ehlers-danlos syndrome report of case. J. Oral Surg. 659-661, 1969.  
    http://www.epub.org.br/ojdom/vol05n03/caso34/danlos1.htm
    
    Extractions: Introduction The Ehlers-Danlos Syndrome represents a group of hereditary changes of the connective tissue, which may be clinically differentiated by inheritance, the ultra structural histology and the biochemical findings. Presently at least 8 forms of the disease are known (from SED I to VIII) with SED I, SED II, SED III being the most common. These are inherited as autosomal dominant disease, but the biochemical bases are unknown, although in each one of them the collagen is abnormal. Clinical Characteristics The clinical characteristics of this disease are: skin hyperelasticity, joint disorders, skin and blood vessel fragility, resulting in contusions, as well as abnormal scars of the cutaneous wounds. The clinical manifestations however may present considerable variation, depending on the patient’s particular syndrome. In case extensibility of the skin is serious, the patient becomes known as the circus “rubber man”. The facies is often typical, like hypertelorism, large nose and lateral folds (wrinkles), being common characteristics. The protrusion of the ears and frontal bossae are frequent. Mobile subcutaneous nodules are often found, and seem to represent fibrosed fat lobules. Scar marks of skin wounds are not common in these patients because the scars spread with time instead of contracting.

75. Ehlers-Danlos Syndrome
    of ehlers-danlos syndrome. 6399 Wilshire Blvd., Suite 510, Los Angeles, CA 90048. (213) 6513038. http//www.ednf.org/. ehlers-danlos syndrome.  
    http://www.arthritis-symptom.com/d-g/ehlers-danlos-syndrome.htm
    
    Extractions: Rheumatoid ... S For more information you can contact Ehlers-Danlos National Foundation. 6399 Wilshire Blvd., Suite 510, Los Angeles, CA 90048. (213) 651-3038. http://www.ednf.org/ 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. Ehlers–Danlos syndrome (EDS) 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 ED

76. Ehlers-Danlos Syndrome In UK Directory: Personal: Genetic Diseases
    ehlersdanlos syndrome. Find general information, support organisations and advice on treatment and symptoms. Ehlers Danlos Syndrome Ehlers Danlos Syndrome.  
    http://www.ukdirectory.co.uk/Dir/?Category=705563,705564,42313,670342,10154547

77. Disease - Ehlers-Danlos Syndrome - Hartford, Connecticut , Saint Francis Care
    Disease ehlers-danlos syndrome. Definition Genetic counseling is recommended for prospective parents with a family history of ehlers-danlos syndrome.  
    http://www.saintfranciscare.com/11884.cfm
    
    Extractions: Back Back to main Health Information page Definition: Ehlers-Danos syndrome is a group of inherited disorders characterized by excessive looseness (laxity) of the joints, hyperelastic skin that is fragile and bruises easily, and/or easily damaged blood vessels. The syndrome sometimes involves rupture of internal organs. Causes And Risk: Ehlers-Danlos syndrome (EDS) can occur in different forms involving vessels, skin, and/or joints with a variety of different genetic defects as their cause. Different forms of EDS have different modes of inheritance. Family history is a risk factor in some cases. Prevention: Genetic counseling is recommended for prospective parents with a family history of Ehlers-Danlos syndrome. Affected parents should be aware of the type of Ehlers-Danlos syndrome they have and its mode of inheritance . This may be determined through testing and evaluation suggested by your health care provider or genetic counselor. Symptoms: Joint dislocation or subluxation Joint pain Increased joint mobility, joints popping, early arthritis

78. EHLERS-DANLOS SYNDROME
    Features Listed For ehlersdanlos syndrome. McKusick Abnormal scar formation; Aneurysms; Blue sclera; Club foot/hindfoot, varus; Detached retina;  
    http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?525

79. EHLERS-DANLOS SYNDROME TYPE VII
    Features Listed For ehlersdanlos syndrome TYPE VII. McKusick 225410. Abnormal labia; Aortic incompetence; Blue sclera; Cranial sutures  
    http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?2327

80. UCSF News Archive: Gene Linked In Ehlers-Danlos Syndrome
    Gene Linked in ehlersdanlos syndrome. FOR IMMEDIATE RELEASE May 7, 1997. UCSF RESEARCHERS FIND GENE LINKED TO CONNECTIVE TISSUE DEFECT IN ehlers-danlos syndrome.  
    http://itssrv1.ucsf.edu/~adcom/listserv/ucsfnews/0089.html

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

61-80 of 103    Back | 1  | 2  | 3  | 4  | 5  | 6  | Next 20