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  2. Hypermobility (joints) - Wikipedia

    en.wikipedia.org/wiki/Hypermobility_(joints)

    Hypermobile joints are common and occur in about 10 to 25% of the population, [3] but in a minority of people, pain and other symptoms are present. This may be a sign of hypermobility spectrum disorder (HSD). Hypermobile joints are a feature of genetic connective tissue disorders such as hypermobility spectrum disorder or EhlersDanlos ...

  3. Ehlers–Danlos syndrome - Wikipedia

    en.wikipedia.org/wiki/EhlersDanlos_syndrome

    In 2018, the EhlersDanlos Society began the Hypermobile EhlersDanlos Genetic Evaluation (HEDGE) study. [22] The ongoing study has screened over 1,000 people who have been diagnosed with hEDS by the 2017 criteria to evaluate their genome for a common mutation.

  4. Hypermobility spectrum disorder - Wikipedia

    en.wikipedia.org/wiki/Hypermobility_spectrum...

    Hypermobility spectrum disorder does not include people with asymptomatic hypermobility or people with double-jointedness but no other symptoms. Hypermobile EhlersDanlos syndrome and hypermobility spectrum disorders may be equally severe. [5] [6] HSD is further classified into different subtypes, which include: [6]

  5. Hypermobility variant of Ehlers–Danlos syndrome - Wikipedia

    en.wikipedia.org/?title=Hypermobility_variant_of...

    Hypermobility variant of EhlersDanlos syndrome. Add languages ... Printable version; In other projects ... Text is available under the Creative Commons Attribution ...

  6. Ehlers-Danlos Society - Wikipedia

    en.wikipedia.org/wiki/Ehlers-Danlos_Society

    The Ehlers–Danlos Society is an international nonprofit organization dedicated to patient support, scientific research, advocacy, and increasing awareness for the EhlersDanlos syndromes (EDS) and hypermobility spectrum disorder (HSD). [1] The society has organized multiple events around the world in an attempt to raise awareness for EDS ...

  7. Bethlem myopathy - Wikipedia

    en.wikipedia.org/wiki/Bethlem_myopathy

    Bethlem myopathy 2 (BTHLM2), formerly known as myopathic-type EhlersDanlos syndrome, is caused by a mutation on the COL12A1 gene coding for type XII collagen. [3] It is autosomal dominant. [3] In 2017, an international workshop proposed a redefined criteria and naming system for limb-girdle muscular dystrophies.

  8. Child Behavior Checklist - Wikipedia

    en.wikipedia.org/wiki/Child_Behavior_Checklist

    The Child Behavior Checklist (CBCL) is a widely used caregiver report form identifying problem behavior in children. [ 1 ] [ 2 ] It is widely used in both research and clinical practice with youths. It has been translated into more than 90 languages, [ 3 ] and normative data are available integrating information from multiple societies.

  9. Category:Ehlers–Danlos syndrome - Wikipedia

    en.wikipedia.org/wiki/Category:EhlersDanlos...

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