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   What is facioscapulohumeral muscular dystrophy (FSHD)?

   • Facioscapulohumeral muscular dystrophy (FSHD) is one of the most common forms of muscular dystrophy (a group of diseases that cause your muscles to become progressively weaker) and can affect both males and females.

   Facioscapulohumeral Muscular Dystrophy (FSHD) - The Loop - Your

   theloopcommunity.org/health-and-wellbeing/conditions/facioscapulohumeral-muscular-dystrophy

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   What are the different types of muscular dystrophies?

   • These include many muscular dystrophies (Duchenne, Becker and Emery-Dreifuss muscular dystrophies, myotonic dystrophy types 1 and 2, limb-girdle muscular dystrophy types 1B, 2C–F, 2G and 2I) (13) and certain congenital myopathies (14). Cardiac involvement may manifest as cardiomyopathy or cardiac arrhythmias (14).

   Physical exercise in adults with hereditary neuromuscular disease

   tidsskriftet.no/en/2018/06/klinisk-oversikt/physical-exercise-adults-hereditary-neuromuscular-disease

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   Can limb girdle muscular dystrophy cause dilated cardiomyopathy?

   • For some neuromuscular diseases such as limb-girdle muscular dystrophy type 1B (laminopathy), cardiac involvement may be the first and sometimes the only sign of neuromuscular disease (13). The most common variant of limb-girdle muscular dystrophy in Norway, type 2I, may give rise to dilated cardiomyopathy and conduction disease (13).

   Physical exercise in adults with hereditary neuromuscular disease

   tidsskriftet.no/en/2018/06/klinisk-oversikt/physical-exercise-adults-hereditary-neuromuscular-disease

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2. tidsskriftet.no › en › 2018Physical exercise in adults with hereditary neuromuscular ...

   tidsskriftet.no › en › 2018

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   3 days ago · These include many muscular dystrophies (Duchenne, Becker and Emery-Dreifuss muscular dystrophies, myotonic dystrophy types 1 and 2, limb-girdle muscular dystrophy types 1B, 2C–F, 2G and 2I) (13) and certain congenital myopathies (14). Cardiac involvement may manifest as cardiomyopathy or cardiac arrhythmias (14).

   • Author: Hanne Ludt Fossmo, Elizabeth Holtebekk, Kaja Giltvedt, Andreas Rosenberger Dybesland, Petter Schandl...

   • Publish Year: 2018

3. www.medscape.org › viewarticle › 744393The Collagen VI-Related Myopathies: Muscle Meets Its Matrix

   www.medscape.org › viewarticle › 744393

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   3 days ago · Differentiating Emery-Dreifuss muscular dystrophy and collagen VI-related myopathies using a specific CT scanner pattern. Neuromuscul. Disord. 20 , 517-523 (2010).

4. mdpi-res.com › d_attachment › ijmsCongenital LMNA-Related Muscular Dystrophy in Paediatrics ...

   mdpi-res.com › d_attachment › ijms

   4 days ago · the LMNA gene give rise to a spectrum of muscular dystrophies characterised by variable dilated cardiomyopathy, collectively referred to as laminopathies. Among these condi-tions are Emery–Dreifuss muscular dystrophy, limb-girdle muscular dystrophy WB, and LMNA-related congenital muscular dystrophy (L-CMD). These laminopathies often ex-

5. Videos

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     What is EDMD? (Emery-Dreifuss Muscular Dystrophy)

     Jul 6, 2015

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     Pronunciation of the word(s) "Emery-Dreifuss Muscular Dystrophy (EDMD)".

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     EDMD- Emery-Dreifuss Muscular Dystrophy simplified

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6. theloopcommunity.org › health-and-wellbeingLimb Girdle Muscular Dystrophy (LGMD) - The Loop - Your ...

   theloopcommunity.org › health-and-wellbeing

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   2 days ago · Mutations in this gene also cause Emery-Dreifuss muscular dystrophy and congenital muscular dystrophy; Usually slow progression; Contractures common; LGMD Type: 1C. Gene affected: caveolin 3 Age of onset: Any age Breathing usually affected: No Heart usually affected: No Comments:

7. people.com › richard-dreyfuss-made-alleged-sexistRichard Dreyfuss' Alleged Sexist, Transphobic Comments at

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   3 days ago · A Jaws screening and Q&A with the film's star, Richard Dreyfuss, in Massachusetts ended in walkouts after the 76-year-old actor allegedly made sexist and transphobic comments. On Saturday, May 25 ...

8. theloopcommunity.org › health-and-wellbeingFacioscapulohumeral Muscular Dystrophy (FSHD) - The Loop ...

   theloopcommunity.org › health-and-wellbeing

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   3 days ago · Understanding FSHD and how it’s diagnosed. Facioscapulohumeral muscular dystrophy (FSHD) is one of the most common forms of muscular dystrophy (a group of diseases that cause your muscles to become progressively weaker) and can affect both males and females.

9. www.scielo.br › j › rppSciELO - Brasil - A rare LMNA missense mutation causing a ...

   www.scielo.br › j › rpp

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   4 days ago · These pieces of evidence probably explain the very different clinical manifestations in this case when compared to the phenotype observed in our patient, as well as in other cases in the literature reported in this study, and the divergent diagnosis established as Emery-Dreifuss muscular dystrophy.