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  2. Ullrich congenital muscular dystrophy - Wikipedia

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

    Ullrich congenital muscular dystrophy; Other names: Scleroatonic muscular dystrophy [1] Autosomal recessive pattern is the inheritance manner of this condition: Symptoms: Muscle weakness [2] Types: UCMD1, UCMD2: Causes: Mutations in the COL6A1, COL6A2, COL6A3, and COL12A1 gene [3] Diagnostic method: Physical exam, Medical history [3] Medication

  3. Duchenne muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Duchenne_muscular_dystrophy

    Duchenne muscular dystrophy is the most common type of muscular dystrophy, [3] with a median life expectancy of 28–30 years. [10] [11] However, with comprehensive care, some individuals may live into their 30s or 40s. [3] Duchenne muscular dystrophy is considerably rarer in females, occurring in approximately one in 50,000,000 live female ...

  4. Muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Muscular_Dystrophy

    Muscular dystrophies (MD) are a genetically and clinically heterogeneous group of rare neuromuscular diseases that cause progressive weakness and breakdown of skeletal muscles over time. [ 1 ] The disorders differ as to which muscles are primarily affected, the degree of weakness, how fast they worsen, and when symptoms begin. [ 1 ]

  5. Myotonic dystrophy - Wikipedia

    en.wikipedia.org/wiki/Myotonic_dystrophy

    DM1 is the most common form of myotonic muscular dystrophy diagnosed in children, with a prevalence ranging from 1 per 100,000 in Japan to 3–15 per 100,000 in Europe. [13] The prevalence may be as high as 1 in 500 in regions such as Quebec, possibly due to the founder effect. The incidence of congenital myotonic dystrophy is thought to be ...

  6. Oculopharyngeal muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Oculopharyngeal_muscular...

    Orthopedic devices for management [1] Oculopharyngeal muscular dystrophy (OPMD) is a rare form of muscular dystrophy with symptoms generally starting when an individual is 40 to 50 years old. It can be autosomal dominant neuromuscular disease or autosomal recessive. The most common inheritance of OPMD is autosomal dominant, which means only one ...

  7. 'Teen Mom's Leah Messer Shares How Daughter Ali Is ... - AOL

    www.aol.com/teen-moms-leah-messer-shares...

    Leah Messer is giving fans an update on her daughter's muscular dystrophy battle. The 29-year-old Teen Mom star took to Instagram on Thursday to reveal that her 12-year-old daughter, Ali, heard ...

  8. Bethlem myopathy - Wikipedia

    en.wikipedia.org/wiki/Bethlem_myopathy

    Bethlem myopathy is a slowly progressive muscle disease characterized predominantly by contractures, rigidity of the spine, skin abnormalities and proximal muscle weakness. [5][11] Symptoms may present as early as infancy, with typical contractures and hyperlaxity of joints; however, in some patients, symptoms may go unnoticed until adolescence ...

  9. Trainers Are Begging You To Do 10 Simple Posture-Fixing Moves

    www.aol.com/lifestyle/trainers-begging-10-simple...

    Time: 20-40 minutes | Equipment: 2 dumbbells, resistance band, 1 kettlebell (can be modified without equipment) | Good for: upper and lower back muscles, chest muscles (pectorals), shoulders, abs ...