Swipe Left to read all Muscular Dystrophy Articles
Muscular Dystrophy
Distal muscular dystrophy is the name of a group of progressive disorders that leads to weakness in the distal muscles. Distal muscular dystrophy (DD), also called distal myopathy, is not one disorder, but a group of genetic disorders under the larger umbrella of muscular dystrophy. DD is marked by progressive weakness and/or wasting of the voluntary distal
Muscular dystrophy life expectancy varies significantly based on disease type. Some have a normal life span, while others have a reduced life span. Muscular dystrophies are a group of genetic diseases that impact the functioning of muscles. There are several variants of muscular dystrophy and each carries a different prognosis. Since each muscular dystrophy is unique, there are different life
Duchenne muscular dystrophy is a progressive, usually fatal, genetic disorder that causes muscle weakness. Find out more. Duchenne muscular dystrophy (DMD) is a severe, progressive neuromuscular disease that affects the muscles. Caused by a defective gene and first appearing in childhood, DMD results in weakness and muscle loss that gets worse over time.How Common Is
Facioscapulohumeral muscular dystrophy causes progressive muscle damage but is not as severe as other muscular dystrophies. Learn more. Facioscapulohumeral muscular dystrophy (FSHD) is the third most common type of muscular dystrophy. Although it also causes progressive muscle weakness, FSHD does not shorten your life expectancy as other forms of muscular dystrophy do.Named after
What to Know About Muscular Dystrophy in Children As a Parent
Signs of muscular dystrophy in children appear around age 2-5 when a child starts to walk. Learn how to cope as a parent and help your child live comfortably. Muscular dystrophy (MD) is a group of rare genetic diseases that lead to weakened and abnormal muscle function over time. Although the age of diagnosis can vary from infancy to adulthood, the average age of diagnosis is 5 years old. Parents and
Congenital muscular dystrophy is an umbrella term for a category of genetic muscle diseases seen either at birth or shortly after. Congenital muscular dystrophy (CMD) is the name for a category of genetic muscle diseases that first appear near birth or within two years of life. It’s an umbrella term for more than 30 conditions, which can cause a range of symptoms. Generally,
Myotonic muscular dystrophy is a hereditary condition characterized by muscle problems and sometimes other health issues. Learn more about symptoms and treatment. Myotonic muscular dystrophy, which is sometimes called myotonic dystrophy, is a type of muscular dystrophy. It is estimated that the condition affects about one in 8,000 people worldwide. There are two types of myotonic muscular dystrophy, described
What are the causes of muscular dystrophy? Learn how genetics plays a role and if there are any risk factors that may cause muscular dystrophy. If you have muscular dystrophy or suspect you have it, you need to check in with your doctor. Properly understanding and treating this disease is paramount to successful management of the condition. And one important component of understanding the
Muscular dystrophy treatment focuses on progression and quality of life. Options can include prescriptions, therapies, devices, and surgery. Unfortunately, there is no known cure for muscular dystrophy (MD), but researchers are making advances that continue to improve the quality of lives of people living with the disease. Today, patients often turn to a variety of conventional and