Category Archives: Muscular Dystrophy Treatment

Review Date: 2/1/2012 Reviewed By: Neil K. Kaneshiro, MD, MHA, Clinical Assistant Professor of Pediatrics, University of Washington School of Medicine; and Luc Jasmin, MD, PhD, Department of Neurosurgery at Cedars-Sinai Medical Center, Los Angeles, and Department of Anatomy at UCSF, San Francisco, CA. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M. Healthcare Solutions, Ebix, Inc. A.D.A.M., Inc. is accredited by URAC, also known as the American Accreditation HealthCare Commission (www.urac.org). URAC's accreditation program is an independent audit to verify that A.D.A.M. follows rigorous standards of quality and accountability. A.D.A.M. is among the first to achieve this important distinction for online health information and services. Learn more about A.D.A.M.'s editorial policy, editorial process and privacy policy. A.D.A.M. is also a founding member of Hi-Ethics and subscribes to the principles of the Health on the Net Foundation (www.hon.ch). A.D.A.M. Copyright The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed medical professional should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information … Continue reading →

At the moment, there is no cure for any of the 9 types of muscular dystrophy. Conventional methods of coping with the disease include exercise, drugs that slow down or eliminate muscle wasting, anabolic steroids and supplementation. These methods are aimed to slow down the progression of the disease, or reduce its symptoms, and usually they are effective in prolonging the lifespan of affected individuals Researchers are already studying gene therapies to treat muscular dystrophies, but the results of this research - if any - will be available no sooner than several years from now Researchers are also investigating the potential of certain muscle building medicines to slow down or reverse the progression of muscular dystrophy. Other trials are looking into the effects of the dietary supplements creatine and glutamine on muscle energy production and storage. Symptoms can often be reduced through exercise, physical therapy, respiratory care, surgery and rehabilitative devices. This can be particularly helpful in minimizing painful positioning of the joints and in preventing or reducing abnormal curvatures of the spine. Walking aids such as canes or wheelchairs can help sufferers maintain mobility and independence. Surgery can help reduce or eliminate muscle shortening (which would otherwise cause a … Continue reading →

Muscular dystrophy (MD) refers to a number of inherited diseases characterized by progressive weakness and wasting of the muscles. The most common MD type is Duchenne's muscular dystrophy. Among others are Becker, limb girdle, congenital, facioscapulohumeral, myotonic, oculopharyngeal, distal, and Emery-Dreifuss MD types. Duchenne muscular dystrophy (DMD) is a hereditary X-linked disease developing as a result of mutation in the dystrophin gene that leads to deficiency of this protein. Dystrofin belongs to the large class of sarcolemmal proteins and glycoproteins. Dystrophin deficiency results in degeneration of cells, especially myocytes, and cells participating in muscle stimulation processes related to contractive activity. Dystrophin deficiency also leads to relaxation of the sarcolemma hitch, which, in turn, results in membrane rupture and launches the sequence of processes resulting in muscle fibre necrosis. The types of MD differ by the location of the muscles affected, the rate of the disease progress, the age the first symptoms appear, etc. For example, the genes for Duchenne's that are X-linked express only in boys but are carried and passed on by women. Boys with Duchenne's MD are usually in a wheelchair by the age of 12 and rarely live past their teens. There is no cure for muscular … Continue reading →

Muscular dystrophy is a group of inherited disorders that involve muscle weakness and loss of muscle tissue, which get worse over time. Muscular dystrophies, or MD, are a group of inherited conditions, which means they are passed down through families. They may occur in childhood or adulthood. There are many different types of muscular dystrophy. They include: Symptoms vary with the different types of muscular dystrophy. All of the muscles may be affected. Or, only specific groups of muscles may be affected, such as those around the pelvis, shoulder, or face. Muscular dystrophy can affect adults, but the more severe forms tend to occur in early childhood. Symptoms include: A physical examination and your medical history will help the doctor determine the type of muscular dystrophy. Specific muscle groups are affected by different types of muscular dystrophy. The doctor's exam may show: Some types of muscular dystrophy involve the heart muscle, causing cardiomyopathy or disturbed heart rhythm (arrhythmias). Often, there is a loss of muscle mass (wasting), which may be hard to see because some types of muscular dystrophy cause a buildup of fat and connective tissue that makes the muscle appear larger. This is called pseudohypertrophy. A muscle biopsy … Continue reading →

Muscular dystrophy is a group of inherited disorders that involve muscle weakness and loss of muscle tissue, which get worse over time.A.D.A.M. Muscular dystrophies, or MD, are a group of inherited conditions, which means they are passed down through families. They may occur in childhood or adulthood. There are many different types of muscular dystrophy. They include: Symptoms vary with the different types of muscular dystrophy. All of the muscles may be affected. Or, only specific groups of muscles may be affected, such as those around the pelvis, shoulder, or face. Muscular dystrophy can affect adults, but the more severe forms tend to occur in early childhood. Symptoms include: A physical examination and your medical history will help the doctor determine the type of muscular dystrophy. Specific muscle groups are affected by different types of muscular dystrophy. The doctor's exam may show: Some types of muscular dystrophy involve the heart muscle, causing cardiomyopathy or disturbed heart rhythm (arrhythmias). Often, there is a loss of muscle mass (wasting), which may be hard to see because some types of muscular dystrophy cause a buildup of fat and connective tissue that makes the muscle appear larger. This is called pseudohypertrophy. A muscle biopsy … Continue reading →

Muscular Dystrophy: Introduction Muscular dystrophy is a progressive genetic disorder that causes deterioration of the muscles and eventually leads to muscle wasting, muscle weakness, bone deformities and disability. The progression and severity of muscular dystrophy varies greatly between individuals and the type of muscular dystrophy. There are nine types of muscular dystrophy, also called MD. The two most common types of muscular dystrophy include Duchenne muscular dystrophy and Becker muscular dystrophy. The only difference between the two diseases are that the symptoms of Duchenne muscular dystrophy develop earlier in life and progresses more quickly than they do in Becker muscular dystrophy, which begins about age seven. There are also many muscular diseases that are very similar to muscular dystrophy. General symptoms of muscular dystrophy include muscle weakness and muscle wasting. This is due to the death of muscle cells and tissue, which are then replaced by fat and connective tissue. The muscle weakness often begins in the legs, but the disease eventually progresses to muscles in other parts of the body, resulting in serious complications, including difficulty breathing. Muscular dystrophy is more common in boys than in girls. Symptoms often begin in infancy or early childhood but can start in … Continue reading →

Review Date: 2/1/2012 Reviewed By: Neil K. Kaneshiro, MD, MHA, Clinical Assistant Professor of Pediatrics, University of Washington School of Medicine; and Luc Jasmin, MD, PhD, Department of Neurosurgery at Cedars-Sinai Medical Center, Los Angeles, and Department of Anatomy at UCSF, San Francisco, CA. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M. Healthcare Solutions, Ebix, Inc. A.D.A.M., Inc. is accredited by URAC, also known as the American Accreditation HealthCare Commission (www.urac.org). URAC's accreditation program is an independent audit to verify that A.D.A.M. follows rigorous standards of quality and accountability. A.D.A.M. is among the first to achieve this important distinction for online health information and services. Learn more about A.D.A.M.'s editorial policy, editorial process and privacy policy. A.D.A.M. is also a founding member of Hi-Ethics and subscribes to the principles of the Health on the Net Foundation (www.hon.ch). A.D.A.M. Copyright The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed medical professional should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information … Continue reading →

The muscular dystrophies (MD) are a group of more than 30 genetic diseases characterized by progressive weakness and degeneration of the skeletal muscles that control movement. Some forms of MD are seen in infancy or childhood, while others may not appear until middle age or later. The disorders differ in terms of the distribution and extent of muscle weakness (some forms of MD also affect cardiac muscle), age of onset, rate of progression, and pattern of inheritance. Duchenne MD is the most common form of MD and primarily affects boys. It is caused by the absence of dystrophin, a protein involved in maintaining the integrity of muscle. Onset is between 3 and 5 years and the disorder progresses rapidly. Most boys are unable to walk by age 12, and later need a respirator to breathe. Girls in these families have a 50 percent chance of inheriting and passing the defective gene to their children. Boys with Becker MD (very similar to but less severe than Duchenne MD) have faulty or not enough dystrophin. Facioscapulohumeral MD usually begins in the teenage years. It causes progressive weakness in muscles of the face, arms, legs, and around the shoulders and chest. It progresses … Continue reading →

Muscular dystrophy (MD) is a group of muscle diseases that weaken the musculoskeletal system and hamper locomotion.[1][2] Muscular dystrophies are characterized by progressive skeletal muscle weakness, defects in muscle proteins, and the death of muscle cells and tissue.[3] In the 1860s, descriptions of boys who grew progressively weaker, lost the ability to walk, and died at an early age became more prominent in medical journals. In the following decade, French neurologist Guillaume Duchenne gave a comprehensive account of thirteen boys with the most common and severe form of the disease, which now carries his nameDuchenne muscular dystrophy. It soon became evident that the disease had more than one form. The other major forms are Becker, limb-girdle, congenital, facioscapulohumeral, myotonic, oculopharyngeal, distal, and Emery-Dreifuss muscular dystrophy.[4] Duchenne and Becker muscular dystrophies, being caused by a mutation of a gene located on the X chromosome, predominantly affect males, although females can sometimes have severe symptoms as well. Most types of MD are multi-system disorders with manifestations in body systems including the heart, gastrointestinal system, nervous system, endocrine glands, eyes and brain.[4] Apart from the nine major types of muscular dystrophy listed above, several MD-like conditions have also been identified. Normal intellectual, behavioral, … Continue reading →

How is Muscular Dystrophy Diagnosed? Muscular dystrophy (MD) is diagnosed through a physical exam, a family medical history, and tests. These might include: For Duchenne and Becker muscular dystrophies, muscle biopsy may show whether dystrophin, a muscle protein, is missing or abnormal, and DNA testing is used to analyze the condition of the related gene. Genetic testing also is available for some forms of muscular dystrophy. There is no cure for any form of muscular dystrophy, but medications and therapy can slow the course of the disease. Human trials of gene therapy with the dystrophin gene are on the near horizon. For instance, scientists are researching ways to insert a working dystrophin gene into the muscles of boys with Duchenne and Becker muscular dystrophies. Researchers are investigating the potential of certain muscle-building medicines to slow down or reverse the progression of muscular dystrophy. Other trials are looking into the effects of the dietary supplements creatine and glutamine on muscle energy production and storage. Symptoms often can be relieved through exercise, physical therapy, rehabilitative devices, respiratory care, and surgery: In some cases, disease progression can be slowed or symptoms relieved with medication: Medications also can be prescribed for some muscular dystrophy-related … Continue reading →