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  2. Mom Has 3 Days to Get Son Life-Saving Treatment for Muscular ...

    www.aol.com/mom-3-days-son-life-150759249.html

    “Duchenne muscular dystrophy (DMD) is one of the most severe forms of inherited muscular dystrophies,” the National Library of Medicine says. “Mutations in the dystrophin gene lead to ...

  3. Delandistrogene moxeparvovec - Wikipedia

    en.wikipedia.org/wiki/Delandistrogene_moxeparvovec

    Delandistrogene moxeparvovec, sold under the brand name Elevidys, is a recombinant gene therapy used for the treatment of Duchenne muscular dystrophy. [3] It is designed to deliver into the body a gene that leads to production of Elevidys micro-dystrophin that contains selected domains of the dystrophin protein present in normal muscle cells. [3]

  4. Myostatin inhibitor - Wikipedia

    en.wikipedia.org/wiki/Myostatin_inhibitor

    Clinical trials for muscular dystrophy have not proven successful in generating functional improvements compared to placebo. Gains of muscle mass were small to non-existent in this population. [13] Research is ongoing on the potential use of myostatin inhibitors for motor neuron diseases like spinal muscle atrophy and amyotrophic lateral ...

  5. Adenosine monophosphate deaminase deficiency type 1

    en.wikipedia.org/wiki/Adenosine_monophosphate...

    The disease was formerly known as myoadenylate deaminase deficiency (MADD). In virtually all cases, the deficiency has been caused by an SNP mutation, known as rs17602729 or C34T . While it was initially regarded as a recessive (or purely homozygous ) disorder, some researchers have reported the existence of similarly deleterious effects from ...

  6. Woman with Muscular Dystrophy Says She Was Dropped ... - AOL

    www.aol.com/lifestyle/woman-muscular-dystrophy...

    Related: Mom Has 3 Days to Get Son Life-Saving Treatment for Muscular Dystrophy Before He's Ineligible (Exclusive) Things only worsened for Morton on her way back to Washington, D.C., on Dec. 2 ...

  7. Calpainopathy - Wikipedia

    en.wikipedia.org/wiki/Calpainopathy

    Calpainopathy is the most common type of autosomal recessive limb-girdle muscular dystrophy (LGMD). [2] It preferentially affects the muscles of the hip girdle and shoulder girdle. No disease modifying pharmaceuticals have been developed as of 2019, although physical therapy, lifestyle modification, and orthopedic surgery can address symptoms.

  8. Dystrophinopathy - Wikipedia

    en.wikipedia.org/wiki/Dystrophinopathy

    Dystrophinopathy refers to a spectrum of diseases due to mutations in the DMD gene, which encodes for the dystrophin protein found in muscle. [ 1 ] [ 2 ] [ 3 ] The severe end of the spectrum includes Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), and DMD -associated dilated cardiomyopathy .

  9. Myostatin - Wikipedia

    en.wikipedia.org/wiki/Myostatin

    Furthermore, individuals who have mutations in both copies of the myostatin gene (popularly—but inaccurately—called the "Hercules gene") have significantly more muscle mass and are stronger than normal. There is hope that studies into myostatin may have therapeutic application in treating muscle wasting diseases such as muscular dystrophy. [12]

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