Definition - Muscular dystrophy is a genetic mutation where the muscle fibres become susceptible to damages causing the muscle to progressively get weaker. Eventually muscular dystrophy will cause the inheritance of this disease to need a wheelchair. Muscular dystrophy is most commonly found in boy and in their early childhood years, other types of muscular dystrophy don’t surface until adulthood.
Duchenne muscular dystrophy symptoms include; Frequent falls, difficulty getting up from a lying or sitting position, trouble running and jumping, waddling gait, large calf muscles and learning disabilities Symptoms - The two most common muscle dystrophies are Duchenne and Becker Muscular Dystrophy. Other more rarer muscular dystrophies include Myotonic, Limb-girdle, Congenital, Fascioscapulohumeral (FSHD) and Oculopharyngeal. (RIGHT BEFORE BECKER MUSCULAR DYSTROPHY)
Becker muscular dystrophy has a variety of signs and symptoms similar to Duchenne muscular dystrophy, but they typically are milder and progress more slowly. Symptom onset is generally in the teens but may not occur until the mid-20s or even later. DUCHENE DYSTROPHY: LOOK UP
Myotonic. Also known as Steinert's disease, this form of muscular dystrophy also features an inability to relax muscles at will. It most often begins in early adulthood. Muscles of the face are usually the first to be affected. Limb-girdle. The hip and shoulder muscles are usually the first affected in this type of muscular dystrophy. In some cases, it becomes difficult to lift the front part of the foot, so frequent tripping may occur. Signs and symptoms may begin from early childhood to adulthood. Congenital. This category of muscular dystrophy is apparent at birth or becomes evident before age 2. Some forms progress slowly and cause only mild disability, while others progress rapidly and cause severe impairment. Fascioscapulohumeral (FSHD). One of the most striking signs of this variety of muscular dystrophy is that the...
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