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  2. Gowers's sign - Wikipedia

    en.wikipedia.org/wiki/Gowers's_sign

    Duchenne muscular dystrophy Gowers's sign is a medical sign that indicates weakness of the proximal muscles , namely those of the lower limb . The sign describes a patient that has to use their hands and arms to "walk" up their own body from a squatting position due to lack of hip and thigh muscle strength.

  3. GALS screen - Wikipedia

    en.wikipedia.org/wiki/GALS_screen

    • The pGALS screen includes three questions relating to pain and function although a negative response does not exclude significant musculoskeletal disease and at a minimum the screening examination should be done in all clinical scenarios where musculoskeletal disease is a concern.

  4. Duchenne muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Duchenne_muscular_dystrophy

    Duchenne muscular dystrophy is a rare progressive disease that eventually affects all voluntary muscles and involves the heart and breathing muscles in later stages. Life expectancy is estimated to be around 25–26, [18] [59] but this varies. People born with Duchenne muscular dystrophy after 1990 have a median life expectancy of approximately ...

  5. Muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Muscular_Dystrophy

    Many affected people will eventually become unable to walk [2] and Duchenne muscular dystrophy in particular is associated with shortened life expectancy. Muscular dystrophy was first described in the 1830s by Charles Bell. [2] The word "dystrophy" comes from the Greek dys, meaning "no, un-" and troph-meaning "nourish". [2]

  6. 6 Self-Screening Questions You Can Ask to Determine If You ...

    www.aol.com/lifestyle/6-self-screening-questions...

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  7. Ullrich congenital muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Ullrich_congenital...

    In terms of the diagnosis of Ullrich congenital muscular dystrophy upon inspection follicular hyperkeratosis, may be a dermatological indicator, additionally also serum creatine kinase may be mildly above normal. [6] Other exams/methods to ascertain if the individual has Ullrich congenital muscular dystrophy are: [medical citation needed] MRI

  8. Congenital muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Congenital_muscular_dystrophy

    Congenital muscular dystrophies are autosomal recessively-inherited muscle diseases.They are a group of heterogeneous disorders characterized by muscle weakness which is present at birth and the different changes on muscle biopsy that ranges from myopathic to overtly dystrophic due to the age at which the biopsy takes place.

  9. Facioscapulohumeral muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Facioscapulohumeral...

    Facioscapulohumeral muscular dystrophy (FSHD) is a type of muscular dystrophy, a group of heritable diseases that cause degeneration of muscle and progressive weakness. Per the name, FSHD tends to sequentially weaken the muscles of the face, those that position the scapula, and those overlying the humerus bone of the upper arm.