Muscular Dystrophy Research Paper

Muscular Dystrophy Research Paper-25
This type of muscular dystrophy is the most common among children. The life expectancy for those with this disease is late teens or 20s.Becker muscular dystrophy is similar to Duchenne muscular dystrophy, but it’s less severe.Congenital muscular dystrophies are often apparent between birth and age 2.

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This type of muscular dystrophy usually begins in your shoulders and hips, but it may also occur in your legs and neck.

You may find it hard to get up out of a chair, walk up and down stairs, and carry heavy items if you have limb-girdle muscular dystrophy. Limb-girdle muscular dystrophy affects both males and females.

Other symptoms of Becker muscular dystrophy include: Many with this disease don’t need a wheelchair until they’re in their mid-30s or older, and a small percentage of people with this disease never require one.

Most people with Becker muscular dystrophy live until middle age or later.

This type of muscular dystrophy also more commonly affects boys.

Muscle weakness occurs mostly in your arms and legs, with symptoms appearing between age 11 and 25.Symptoms vary and may include: While symptoms vary from mild to severe, the majority of people with congenital muscular dystrophy are unable to sit or stand without help.The lifespan of someone with this type also varies, depending on the symptoms.Emery-Dreifuss muscular dystrophy tends to affect more boys than girls.This type of muscular dystrophy usually begins in childhood.Myotonic dystrophy diagnoses are most common in adults in their 20s and 30s. Some people experience mild symptoms, while others have potentially life-threatening symptoms involving the heart and lungs.Facioscapulohumeral muscular dystrophy (FSHD) is also known as Landouzy-Dejerine disease.Most people with this form of muscular dystrophy are disabled by age 20. Oculopharyngeal muscular dystrophy causes weakness in your facial, neck, and shoulder muscles.Other symptoms include: It may also affect your respiratory system and heart muscles.There are more than 30 different types of muscular dystrophy, which vary in symptoms and severity.There are nine different categories used for diagnosis. The symptoms include: People with Duchenne muscular dystrophy typically require a wheelchair before their teenage years.

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    Myotonic dystrophy is a disease that affects the muscles and other body systems. It is the most common form of muscular dystrophy that begins in adulthood, usually in a person’s 20s or 30s.…

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    Find out about the latest research news below and also visit our Breaking News in Research page. Genetic factors that determine the severity of myotonic dystrophy type 1 Researchers involved in the OPTIMISTIC trial have published a scientific paper that identifies genetic factors that influence the severity of myotonic dystrophy type 1.…

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    Muscular Dystrophy Roots, Cause, and Current Research - Muscular Dystrophy Roots, Cause, and Current Research Muscular dystrophy is an inherited disease that was discovered in 1861, by Guillaume B. A. Duchenne. Muscular dystrophy is a group of heredity disorders characterized by rapidly-worsening muscle weakness.…

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