Research Paper On Ehlers Danlos Syndrome

Research Paper On Ehlers Danlos Syndrome-40
To gain further insight into the phenotype of HMS/EDS-HT and its mechanisms, clearer descriptions of these populations should be made available.Future research and clinical care should revise and create consensus on the diagnostic criteria for HMS/EDS-HT (Solution 1), account for clinical heterogeneity by the classification of subtypes within the HMS/EDS-HT spectrum (Solution 2), and create a clinical core set (Solution 3).

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Medical records from other institutions and clinical notes for visits in Dr.

Both physicians combined the pertinent features of the syndrome and accurately delineated the phenotypic features of this group of inherited disorders.

The name, Ehlers-Danlos syndrome, was coined in 1936.

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Wiley Online Library requires cookies for authentication and use of other site features; therefore, cookies must be enabled to browse the site.People with lax joints and multiple scars were first described in the medical writings of Hippocrates, dating back to 400 BCE. His work reports the first detailed clinical description of EDS.The syndrome derives its name from additional clinical case reports presented by 2 physicians: Edvard Ehlers, a Danish dermatologist, in 1901, and Henri-Alexandre Danlos, a French physician with expertise in chemistry of skin disorders, in 1908.Depending on the type, EDS can be diagnosed through laboratory studies or clinical examination.Once the syndrome has been diagnosed, preventative measures should be taken. Tschernogobow, a Russian dermatologist, presented 2 case studies of patients to the Moscow Venereology and Dermatology Society who had marked loose fragile skin, and hypermobile large joints.Holick's clinic will be reviewed to obtain the following information: previous diagnosis at other institutions, age, clinical signs and symptoms of EDS, Joints Hypermobility Syndrome (JHS), and other metabolic or genetic disorders and laboratory results, radiology reports and images, and genetic testing that supports EDS diagnoses. Accepted for publication 11 June 2015 Published 20 August 2015 Volume 2015:8 Pages 591—601 DOI https://doi.org/10.2147/JPR.However, within the Ehlers–Danlos spectrum, a similar subcategory of patients having similar clinical features as HMS but lacking a specific genetic profile was identified: Ehlers–Danlos syndrome hypermobility type (EDS-HT).Researchers and clinicians have struggled for decades with the highly diverse clinical presentation within the HMS and EDS-HT phenotypes (Challenge 1) and the lack of understanding of the pathological mechanisms that underlie the development of pain and its persistence (Challenge 2).Keywords: chronic musculoskeletal pain, generalized joint hypermobility, hypermobility syndrome, Ehlers–Danlos hypermobility type This work is published and licensed by Dove Medical Press Limited.The full terms of this license are available at https:// incorporate the Creative Commons Attribution - Non Commercial (unported, v3.0) License. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.

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  • PDF Ehlers-Danlos syndrome - Share and discover research
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    PDF Ehlers-Danlos syndrome EDS is a generalized disorder of one element of connective tissue manifesting clinically by fragility and hyperelasticity of the skin and joint laxity. It is a.…

  • Ehlers Danlos Syndromes Toolkit - uk
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    The Ehlers-Danlos syndromes EDS are heritable connective tissue disorders affecting the quality of collagen in every part of the body. They were once considered to be very rare and only seen by rheumatologists. There are 13 types of Ehlers-Danlos syndrome, most of which are indeed rare.…

  • Ehlers-Danlos syndrome - Genetics Home Reference - NIH
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    Ehlers-Danlos syndrome is a group of disorders that affect connective tissues supporting the skin, bones, blood vessels, and many other organs and tissues. Defects in connective tissues cause the signs and symptoms of these conditions, which range from mildly loose joints to life-threatening complications.…

  • Ehlers-Danlos syndrome - Doctors and departments - Mayo Clinic
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    Research and Clinical TrialsSee how Mayo Clinic research and clinical trials advance the science of medicine and improve patient care. Explore now. Education. See a list of publications on Ehlers-Danlos syndrome by Mayo Clinic doctors on PubMed, a service of the National Library of Medicine. By Mayo Clinic Staff.…

  • PDF Hypermobile Ehlers Danlos Syndrome -
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    PDF Efforts on recognition, diagnosis and management of the presumed, most common connective tissue disorder, Hypermobile Ehlers Danlos syndrome have…

  • Ehlers Danlos Syndromes - NORD National Organization for.
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    NORD gratefully acknowledges Xenia Chepa-Lotrea, NIH/National Human Genome Research Institute, MD candidate at Georgetown University School of Medicine, and Clair Francomano, MD, Director of Adult Genetics and Director the Ehlers-Danlos National Foundation Center for Clinical Care and Research, Greater Baltimore Medical Center, Harvey Institute for Human Genetics, for assistance in the.…

  • Ehlers-Danlos syndrome - nih.gov
    Reply

    Ehlers-Danlos syndrome EDS is a generalized disorder of one element of connective tissue manifesting clinically by fragility and hyperelasticity of the skin and joint laxity. It is a hereditary disorder, the inheritance being usually autosomal dominant with low penetrance. Autosomal recessive and.…

  • Research - Ehlers Danlos Syndrome Network C. A. R. E. S.
    Reply

    Ehlers Danlos Syndrome is a genetic connective tissue disorder. It affects all the connective tissue throughout our body. Muscles, ligaments, tendons, arteries and skin are like tissue paper.…

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