May. 14, 2023
At vero eos et accusamus et iusto odio dignissimos ducimus qui blanditiis praesentium voluptatum deleniti atque corrupti quos dolores et quas.
Muscular dystrophy (MD) refers to a group of more than 30 genetic diseases that cause progressive weakness and degeneration of skeletal muscles used during voluntary movement. These disorders vary in age of onset, severity, and pattern of affected muscles. All forms of MD grow worse as muscles progressively degenerate and weaken. Many individuals eventually lose the ability to walk.
Some types of MD also affect the:
Respiratory and cardiac diseases may occur, and some people may develop a swallowing disorder. MD is not contagious and cannot be brought on by injury or activity.
How MD affects muscles. Muscles are made up of thousands of muscle fibers. Each fiber is actually a number of individual cells that have joined together during development and are encased by an outer membrane. Muscle fibers that make up individual muscles are bound together by connective tissue.
Muscles are activated when an impulse, or signal, is sent from the brain through the spinal cord and peripheral nerves (nerves that connect the central nervous system to sensory organs and muscles) to the neuromuscular junction (the space between the nerve fiber and the muscle it activates). There, the chemical acetylcholine triggers a series of events that cause the muscle to contract.
The muscle fiber membrane contains a group of proteins, or the dystrophin-glycoprotein complex, that prevent damage when muscle fibers contract and relax. When this protective membrane is damaged, muscle fibers begin to leak the protein creatine kinase, which is needed for the chemical reactions that produce energy for muscle contractions, and take on excess calcium that causes further harm. Affected muscle fibers eventually die from this damage, leading to progressive muscle degeneration.
Although MD can affect several body tissues and organs, it most prominently affects the integrity of muscle fibers. The disease causes:
Also, overall muscle strength and tendon reflexes are usually lessened or lost due to replacement of muscle by connective tissue and fat.
Who is more likely to get muscular dystrophy?
MD occurs worldwide and affects all races. Its incidence varies as some forms are more common than others. Some types of MD are more prevalent in certain countries and regions of the world. Many muscular dystrophies are familial, meaning there is some family history of the disease.
All of the muscular dystrophies are inherited and involve a gene mutation (defect). The body's cells don't work properly when a protein is altered or produced in insufficient quantity (or sometimes missing completely). Many cases of MD occur from spontaneous mutations that are not found in the genes of either parent, and this can be passed to the next generation.
Genes are like blueprints; they contain coded messages that determine a person's characteristics or traits. They are arranged along 23 rod-like pairs of chromosomes with one half of each pair being inherited from each parent. Each half of a chromosome pair is similar to the other, except for one pair, which determines the sex of the individual. Muscular dystrophies can be inherited in three ways:
Similar conditions. There are many other heritable diseases that affect muscles, nerves, or the neuromuscular junction. Diseases like inflammatory myopathy, progressive muscle weakness, and cardiomyopathy (heart muscle weakness that interferes with pumping ability) may produce symptoms that are very similar to those found in some forms of MD, but they are caused by different genetic defects. Disorders with symptoms similar to MD include:
The sharing of symptoms among multiple neuromuscular diseases, and the prevalence of sporadic cases in families not previously affected by MD, often makes it difficult for people with MD to obtain a quick diagnosis. Some individuals may have signs of MD but carry none of the currently recognized genetic mutations.
Classifying muscular dystrophy. There are nine major groups of the muscular dystrophies. The disorders are classified by the:
Although some forms of MD become apparent in infancy or childhood, others may not appear until middle age or later. Overall, incidence rates and severity vary, but each of the dystrophies causes progressive skeletal muscle deterioration, and some types affect cardiac muscle.
Duchenne muscular dystrophy is the most common childhood form of MD, as well as the most common of the muscular dystrophies overall, accounting for approximately 50 percent of all cases. Because inheritance is X-linked recessive (caused by a mutation on the X chromosome), Duchenne MD primarily affects males, although females who carry the defective gene may show some symptoms. About one-third of the cases reflect new mutations and the rest run in families. Female siblings of male children with Duchenne MD have a 50 percent chance of carrying the defective gene. The disorder gets its name from the French neurologist Guillaume Duchenne. Duchenne MD results from an absence of the muscle protein dystrophin. Dystrophin is a protein found in muscle that helps muscles stay healthy and strong. Blood tests of children with Duchenne MD show an abnormally high level of creatine kinase; this finding is apparent from birth. Duchenne MD usually becomes apparent during the toddler years, sometimes soon after an affected child begins to walk. Progressive weakness and muscle wasting (a decrease in muscle strength and size) caused by degenerating muscle fibers begins in the upper legs and pelvis before spreading into the upper arms. Other symptoms include:
Many children are unable to run or jump. The wasting muscles, in particular the calf muscles, and less commonly, muscles in the buttocks, shoulders, and arms, may be enlarged by an accumulation of fat and connective tissue, causing them to look larger and healthier than they actually are (pseudohypertrophy). As the disease progresses, the muscles in the diaphragm that assist in breathing and coughing may weaken. Individuals may experience breathing difficulties, respiratory infections, and swallowing problems. Bone thinning and scoliosis (curving of the spine) are common. Some children have varying degrees of cognitive and behavioral impairments.
Between ages 3 and 6, children may show brief periods of physical improvement followed by progressive muscle degeneration later. Children with Duchenne MD typically lose the ability to walk by early adolescence. Improvements in multidisciplinary care have extended the life expectancy and improved the quality of life significantly for children with Duchenne MD. Numerous individuals survive into their 30s, and some even into their 40s.
Becker muscular dystrophy is less severe than but closely related to Duchenne MD. People with Becker MD have partial but insufficient function of the protein dystrophin. The disorder usually appears around age 11 but may occur as late as age 25, and affected individuals generally live into middle age or later. The rate of progressive, symmetric (on both sides of the body) muscle atrophy and weakness varies greatly among affected individuals. Many individuals are able to walk until they are in their mid-30s or later, while others are unable to walk past their teens. Some affected individuals never need to use a wheelchair. As in Duchenne MD, muscle weakness in Becker MD is typically noticed first in the upper arms and shoulders, upper legs, and pelvis.
Early symptoms of Becker MD include:
Calf muscles may appear large and healthy as deteriorating muscle fibers are replaced by fat, and muscle activity may cause cramps in some people. Cardiac complications are not as consistently present in Becker MD compared to Duchenne MD, but may be as severe in some cases. Cognitive and behavioral impairments are not as common or severe as in Duchenne MD, but they do occur.
Congenital muscular dystrophy refers to a group of autosomal recessive muscular dystrophies that are either present at birth or become evident before age 2. The degree and progression of muscle weakness and degeneration vary with the type of disorder. Weakness may be first noted when children fail to meet landmarks in motor function and muscle control. Muscle degeneration may be mild or severe and is restricted primarily to skeletal muscle. The majority of individuals are unable to sit or stand without support, and some affected children may never learn to walk. There are three groups of congenital MD:
Defects in the protein merosin cause nearly half of all cases of congenital MD.
People with congenital MD may develop:
The intellectual development of some children progresses as expected, while others become severely impaired. Weakness in diaphragm muscles may lead to respiratory failure. Congenital MD may also affect the central nervous system, causing vision and speech problems, seizures, and structural changes in the brain.
Distal muscular dystrophy (also known as distal myopathy) describes a group of at least six specific muscle diseases that primarily affect distal muscles (those farthest away from the shoulders and hips) in the forearms, hands, lower legs, and feet. Distal dystrophies are typically less severe, progress more slowly, and involve fewer muscles than other forms of MD, although they can spread to other muscles, including the proximal ones later in the course of the disease. Distal MD can affect the heart and respiratory muscles, and individuals may eventually require the use of a ventilator. They may not be able to perform fine hand movement and have difficulty extending the fingers. As leg muscles become affected, walking and climbing stairs become difficult and some people may be unable to hop or stand on their heels.
Onset of distal MD, which affects both males and females, is typically between the ages of 40 and 60 years. In one form of distal MD, a muscle membrane protein complex called dysferlin is known to be lacking.
Although distal MD is primarily an autosomal dominant disorder, autosomal recessive forms have been reported in young adults. Symptoms are similar to those of Duchenne MD but with a different pattern of muscle damage. An infantile-onset form of autosomal recessive distal MD has also been reported. Slow but progressive weakness is often first noticed around age 1, when the child begins to walk, and continues to progress very slowly throughout adult life.
Emery-Dreifuss muscular dystrophy primarily affects male children. The disorder has two forms: One is X-linked recessive and the other is autosomal dominant.
Onset of Emery-Dreifuss MD is usually apparent by age 10, but symptoms can appear as late as the mid-20s. This disease causes slow yet progressive wasting of the upper arm and lower leg muscles and symmetric weakness. Contractures in the spine, ankles, knees, elbows, and back of the neck usually precede significant muscle weakness, which is less severe than in Duchenne MD. Contractures may cause elbows to become locked in a flexed position. The entire spine may become rigid as the disease progresses. Other symptoms include:
Serum creatine kinase levels may be moderately elevated. Nearly all people with Emery-Dreifuss MD have some form of heart problem by age 30, often requiring a pacemaker or other assistive device. Female carriers of the disorder often have cardiac complications without muscle weakness. In some cases, the cardiac symptoms may be the earliest and most significant symptom of the disease, and may appear years before muscle weakness does.
Facioscapulohumeral muscular dystrophy (FSHD) initially affects muscles of the face (facio), shoulders (scapulo), and upper arms (humera) with progressive weakness. Also known as Landouzy-Dejerine disease, this is the third most common form of MD and is characterized as an autosomal dominant disorder. Most people have a normal life span, but some become severely disabled.
Disease progression is typically very slow, with intermittent spurts of rapid muscle deterioration. Onset is usually in the teens but may occur as early as childhood or as late as age 40. One hallmark of FSHD is that it commonly causes asymmetric weakness. Muscles around the eyes and mouth are often affected first, followed by weakness around the shoulders, chest, and upper arms. A particular pattern of muscle wasting causes the shoulders to appear to be slanted and the shoulder blades to appear winged. Muscles in the lower extremities may also become weakened. Reflexes are diminished, typically in the same distribution as the weakness. Changes in facial appearance may include the development of a crooked smile, a pouting look, flattened facial features, or a mask-like appearance. Some individuals cannot pucker their lips or whistle and may have difficulty swallowing, chewing, or speaking. Muscle weakness can also spread to the diaphragm, causing respiratory problems.
Other symptoms may include:
Contractures are rare. Some people with FSHD feel severe pain in the affected limb. Cardiac muscles are not usually affected, and significant weakness of the pelvis is less common than in other forms of MD. An infant-onset form of FSHD can cause retinal disease and some hearing loss.
Limb-girdle muscular dystrophy (LGMD) refers to more than 20 inherited conditions marked by progressive loss of muscle bulk and symmetrical weakening of voluntary muscles, primarily those in the shoulders and around the hips. At least five forms of autosomal dominant limb-girdle MD (known as type 1) and 17 forms of autosomal recessive limb-girdle MD (known as type 2) have been identified. Some autosomal recessive forms of the disorder are now known to be due to a deficiency of any of four dystrophin-glycoprotein complex proteins called the sarcoglycans. Deficiencies in dystroglycan, classically associated with congenital muscular dystrophies, may also cause LGMD.
The recessive LGMDs occur more frequently than the dominant forms, usually starting in childhood or the teens, and show dramatically increased levels of serum creatine kinase. The dominant LGMDs usually begin in adulthood. In general, the earlier the clinical signs appear, the more rapid the rate of disease progression. Limb-girdle MD affects both males and females. Some forms of the disease progress rapidly, resulting in serious muscle damage and loss of the ability to walk, while others advance very slowly over many years and cause minimal disability, allowing a normal life expectancy. In some cases, the disorder appears to halt temporarily, but progression then resumes.
The pattern of muscle weakness is similar to that of Duchenne MD and Becker MD. Weakness is typically noticed first around the hips before spreading to the shoulders, legs, and neck. Individuals develop a waddling gait and have difficulty when rising from chairs, climbing stairs, or carrying heavy objects. They fall frequently and are unable to run. Contractures at the elbows and knees are rare but individuals may develop contractures in the back muscles, which gives them the appearance of a rigid spine. Proximal reflexes (closest to the center of the body) are often impaired. Some individuals also experience cardiomyopathy and respiratory complications, depending in part on the specific subtype. Intelligence remains in most cases, though exceptions do occur. Many individuals with limb-girdle MD become severely disabled within 20 years of disease onset.
Myotonic dystrophy (DM1), also known as Steinert's disease and dystrophia myotonica, is another common form of MD. Myotonia, or the inability to relax muscles following a sudden contraction, is found only in this form of MD, but is also found in other non-dystrophic muscle diseases. People with DM1 can live a long life, with variable but slowly progressive disability. Typical disease onset is between ages 20 and 30, but childhood onset and congenital onset are well-documented. Muscles in the face and the front of the neck are usually first to show weakness and may produce a hallow temples, drooping facial skin, and a thin neck. Wasting and weakness noticeably affect forearm muscles. DM1 affects the central nervous system and other body systems, including the heart, adrenal glands and thyroid, eyes, and gastrointestinal tract.
Other symptoms include:
Individuals may feel drowsy and have an excessive need for sleep. There is a second form known as myotonic dystrophy type 2 (DM2) that is similar to the classic form, but usually affects proximal muscles more significantly.
This autosomal dominant disease affects both males and females. Females may have irregular menstrual periods and are sometimes infertile. The disease may occur earlier and be more severe in successive generations. A childhood-onset form of myotonic MD may become apparent between ages 5 and 10. Symptoms include:
A female with DM1 can give birth to an infant with a rare congenital form of the disorder. Symptoms at birth may include:
Children with congenital myotonic MD may also experience cognitive impairment and delayed motor development. This severe infantile form of myotonic MD occurs almost exclusively in children who have inherited the defective gene from their female parent, whose symptoms may be so mild that they are sometimes not aware of the disease.
The inherited gene defect that causes DM1 is an abnormally long repetition of a three-letter "word" in the genetic code. In unaffected people, the word is repeated a number of times, but in people with DM1, it is repeated many more times. This triplet repeat gets longer with each successive generation. The triplet repeat mechanism has now been implicated in at least 15 other disorders, including Huntington's disease and the spinocerebellar ataxias.
Oculopharyngeal muscular dystrophy (OPMD) generally begins in the 40s and 50s and affects both males and females. In the U.S., the disease is most common in families of French-Canadian descent as well as among Hispanic residents of northern New Mexico. People first report drooping eyelids, followed by weakness in the facial muscles and pharyngeal muscles in the throat that cause problems with swallowing. The tongue may atrophy and changes to the voice may occur. Eyelids may droop so dramatically that some individuals compensate by tilting back their heads. Affected individuals may have:
Muscle weakness and wasting in the neck and shoulder region is common. Limb muscles may also be affected. People with OPMD may find it difficult to walk, climb stairs, kneel, or bend. The most severely affected will eventually lose the ability to walk.
How is muscular dystrophy diagnosed and treated?
Diagnosing MD. Doctors review an individual's medical history and a complete family history to determine if the muscle disease is secondary to a disease affecting other tissues or organs or is an inherited condition. It is also important to rule out any muscle weakness resulting from prior surgery, exposure to toxins, or current medications that may affect the person's functional status. Thorough clinical and neurological exams can help doctors do the following:
Various laboratory tests may be used to confirm the diagnosis of MD, including:
Treating MD. Available treatments are aimed at keeping people independent for as long as possible and to prevent complications that can arise from weakness, reduced mobility, and cardiac and respiratory difficulties. Treatment may involve a combination of approaches, including physical therapy, drug therapy, and surgery.
What are the latest updates on muscular dystrophy?
The National Institute of Neurological Disorders and Stroke (NINDS), a part of the National Institutes of Health (NIH), supports a broad program of research on muscular dystrophy. NINDS and the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), the National Institute of Child Health and Human Development (NICHD), and the National Heart, Blood, and Lung Institute (NHLBI), lead the MD research efforts conducted at the NIH and at grantee institutions across the country.
The NIH supports a broad range of basic, translational, and clinical research in the muscular dystrophies. Advances in basic research are essential to the basic understanding of each type of MD. While many genes that cause muscular dystrophy still remain to be identified, advances in gene sequencing has aided the identification of genes that may be involved for most types of muscular dystrophy. In turn, new knowledge of specific disease mechanisms is identifying potential targets for therapy development. Research into the underlying disease mechanisms has created new opportunities for therapy development in nearly all types of MD. For example, advances in targeted therapy have led to promising efforts in myotonic dystrophy and facioscapulohumeral muscular dystrophy.
Federal funding, through the NIH and other agencies, as well as the venture philanthropy programs supported by patient advocacy groups, have attracted biotechnology and pharmaceutical firm investments into therapies for the MDs. A variety of strategies are employed in developing new drug and biologic therapies for the range of MDs. Strategies being explored are either specific to a particular type of MD or may address disease progression that may apply to multiple types of MD.
Gene replacement therapy. Gene therapy has the potential to address the primary cause of MD by providing for the production of the missing protein. For muscular dystrophies with central nervous system consequences (congenital muscular dystrophy and myotonic dystrophy), researchers are developing and fine-tuning gene therapy vectors (a way to deliver genetic materials to cells) that can cross the protective blood-brain barrier. Progress in delivery of replacement genes in MD includes considerable refinement of the viral vector types that improve the targeting to skeletal muscle and vascular approaches to deliver replacement gene to most or all skeletal muscles.
Clinical testing of gene therapy strategies in MD has been underway for Duchenne and limb-girdle muscular dystrophy. Injections of gene therapy vectors into single muscles of participants were the first step to establishing safety of the approach. With the support of extensive studies in animal models, clinical trials are now moving toward testing of gene therapy of all muscles of entire limbs, using an isolated vascular delivery approach. If isolated limb delivery approaches prove safe and effective, research will move to systemic delivery of gene therapy vectors so all muscles can be treated simultaneously.
Utrophin is a protein that is closely related to dystrophin and is not affected in the gene mutations that cause Duchenne MD. Targeting increased expression of utrophin may prove a useful approach in treating Duchenne MD. NIH supports both gene therapy and small molecule drug development programs to increase the muscle production of utrophin.
Finally, modifier genes—genes with activities that act to reduce the severity of MD—have been discovered by NIH-funded teams. These genes, including latent TGF binding protein 4 and osteopontin, represent new therapeutic targets to potentially reduce the severity of several types of muscular dystrophy.
Genetic modification therapy to bypass inherited mutations. Most individuals with Duchenne have mutations in the dystrophin gene that cause it to function improperly and stop producing the dystrophin protein. By manipulating the protein synthesis process, production of a gene that either "reads through" or “skips” the genetic mutation can result in at least partial functional dystrophin.
Two strategies are currently under study to bypass dystrophin mutations:
Antisense oligonucleotide technology is also being evaluated for use in myotonic dystrophy, but by a different mechanism than in Duchenne MD. In myotonic dystrophy, long duplications of repetitive DNA sequences lead to production of a toxic RNA that sequesters a splicing regulator, Muscleblind, causing mis-splicing of many genes in muscle and brain. An NINDS and NIAMS-supported project is advancing an oligonucleotide therapeutic designed to degrade the toxic RNA and mitigate the splicing defects. This approach, in partnership with academic investigators and biotechnology and pharmaceutical companies, has the potential to address all people having myotonic dystrophy and is planned to be in clinical trials within the next few years.
Drug-based therapy to delay muscle wasting. Progressive loss of muscle mass is primarily responsible for reduced quality and length of life in MD. Drug treatment strategies designed to slow this muscle degeneration can have substantial impact on quality of life. Similarly, skeletal muscle has the ability to repair itself, but its regeneration and repair mechanisms are progressively depleted during the course of several types of MD. Understanding the repair mechanisms may provide new therapies to slow, and possibly stabilize, muscle degeneration.
Corticosteroids are known to extend the ability of people with Duchenne MD to walk by up to two years, but steroids have substantial side effects and their mechanism of action is unknown. A study funded by NINDS is evaluating drugs and their efficacy and tolerability at different doses in order to determine optimal clinical practice for their use in Duchenne MD. In addition, a biotechnology company supported by the NIH's National Center for Advancing Translational Sciences is developing a modified steroid to increase its efficacy in Duchenne while reducing the side effects that often limit individuals from using corticosteroid therapy.
Preclinical drug development efforts supported by NINDS and NIAMS are developing a peptide therapeutic that has dual activity in mitigating muscle damage due to inflammation and also enhancing muscle regeneration in animal models. Efforts to preserve muscle mass through inhibition of a negative regulator of muscle growth, myostatin, have encountered some roadblocks, including failed clinical trials, but are still under study.
Cell-based therapy. The muscle cells of people with MD often lack a critical protein, such as dystrophin in Duchenne MD or sarcoglycan in some of the limb-girdle MDs. Scientists are exploring the possibility that the missing protein can be replaced by introducing muscle stem cells capable of making the missing protein in new muscle cells. Such new cells would be protected from the progressive degeneration characteristic of MD and potentially restore muscle function in affected persons.
The natural regenerative capacity of muscle provides possibilities for treatment of MD. Researchers have shown that stem cells can be used to deliver a functional dystrophin gene to skeletal muscles of dystrophic mice and dogs. The focus of research has been on identifying the cell types with the highest potential for engraftment and growth of muscle and on strategies to deliver these muscle precursor cells to human skeletal muscles. Overall, cell-based therapeutic approaches are under consideration for multiple types of MD.
Moving forward with research in MD. Until recently, most therapy development programs in MD were focused on Duchenne. With dramatic advances in understanding disease mechanisms, significant therapy development efforts are now being launched in many types of MD. NINDS funding supports teams working on the disease mechanisms in facioscapulohumeral muscular dystrophy, central nervous system involvement in myotonic dystrophy, and on the role of fibrosis in Duchenne MD. Similarly, NIAMS-supported projects are identifying novel therapy development targets that are attracting interest from biotechnology and pharmaceutical companies and will help move toward therapy development programs for all types of MD.
Parallel efforts need to be made in clinical trial readiness, so that clinical trials are feasible when a candidate reaches that stage. Patient registries, natural history studies, biomarker identification, development of clinical trial endpoint measures, and the emergence of standards of care are all essential in supporting clinical trials and are being advanced in several types of muscular dystrophy with the support of both public and private sector partners. The NIH has recently undertaken several new initiatives in training, career development, and research that are targeted toward MD. These advances, along with the NINDS focus on translational and clinical research, will lead to the growth of clinical trials and promising treatment strategies.
Federal commitment to muscular dystrophy. In December 2001, President George W. Bush signed into law the Muscular Dystrophy Community Assistance, Research, and Education Amendments Act of 2001 (the MD CARE Act, Public Law 107-84). The MD-CARE act was reauthorized in 2008.
In response to the MD CARE Act, the NIH formed the Muscular Dystrophy Coordinating Committee to help guide research on MD. The MD Coordinating Committee is made up of physicians, scientists, NIH professional staff, and representatives of other federal agencies and voluntary health organizations with a focus on MD. The purpose of the group is to help NIH add new capabilities to the national effort to understand and treat MD without duplicating existing programs.
The NIH is expanding and intensifying its research efforts on the muscular dystrophies and established the The Wellstone Muscular Dystrophy Research Network in honor of the late Senator Paul D. Wellstone of Minnesota. Established as part of the NIH enhancement and intensification of muscular dystrophy research associated with the MD-CARE Act, the centers are supported by five-year, renewable grants. The following NIH Institutes participate in the Wellstone Centers Program:
Research has led to the discovery of disease mechanisms and improved treatment for many forms of MD. Current research promises to generate further improvements. In the coming years, physicians and affected individuals can look forward to new forms of therapy developed through an understanding of the unique traits of MD.
How can I or my loved one help improve care for people with muscular dystrophy?
Consider participating in a clinical trial so clinicians and scientists can learn more about MD and related disorders. Clinical research uses human volunteers to help researchers learn more about a disorder and perhaps find better ways to safely detect, treat, or prevent disease.
All types of volunteers are needed—those who are healthy or may have an illness or disease—of all different ages, sexes, races, and ethnicities to ensure that study results apply to as many people as possible, and that treatments will be safe and effective for everyone who will use them.
Where can I find more information about muscular dystrophy?
Information may be available from the following organizations and resources:
Centers for Disease Control and Prevention (CDC)
Phone: 800-311-3435 or 404-639-3311
Coalition to Cure Calpain 3
Facioscapulohumeral Muscular Dystrophy (FSH) Society
Muscular Dystrophy Association
Myotonic Dystrophy Foundation
Phone: 866-968-6642; 415-800-7777
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Phone: 301-496-8190 or 877-226-4267
National Institute of Child Health and Human Development (NICHD)
Parent Project Muscular Dystrophy (PPMD)
Content source: https://www.ninds.nih.gov/health-information/disorders/muscular-dystrophy Accessed July 13, 2023.
The information in this document is for general educational purposes only. It is not intended to substitute for personalized professional advice. Although the information was obtained from sources believed to be reliable, MedLink, its representatives, and the providers of the information do not guarantee its accuracy and disclaim responsibility for adverse consequences resulting from its use. For further information, consult a physician and the organization referred to herein.