Muscular dystrophy is a group of inherited diseases that cause the voluntary muscles to progressively weaken over time. There are nine main types of muscular dystrophy that can affect any age or gender. Symptoms include muscle weakness, spasms, and difficulty with mobility. While there is no cure, treatment aims to relieve symptoms and slow progression through medications, therapy, exercise, and assistive devices. Researchers are working to develop new treatments like gene therapy.
What is Muscular Dystrophy?
Types of Muscular Dystrophy
What is Duchenne muscular dystrophy (DMD), pathophysiology, clinical presentation, Gowers sign, DMD and Becker's muscular dystrophy and functional grades
Muscular dystrophy is a group of diseases that cause progressive weakness and loss of muscle mass. In muscular dystrophy, abnormal genes (mutations) interfere with the production of proteins needed to form healthy muscle.
What is Muscular Dystrophy?
Types of Muscular Dystrophy
What is Duchenne muscular dystrophy (DMD), pathophysiology, clinical presentation, Gowers sign, DMD and Becker's muscular dystrophy and functional grades
Muscular dystrophy is a group of diseases that cause progressive weakness and loss of muscle mass. In muscular dystrophy, abnormal genes (mutations) interfere with the production of proteins needed to form healthy muscle.
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Lumbar spondylosis- Diagnosis | management | a brief medical study martinshaji
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Amyotrophic lateral sclerosis (ALS), AKA "Lou Gehrig's Disease," is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Motor neurons reach from the brain to the spinal cord and from the spinal cord to the muscles throughout the body. The progressive degeneration of the motor neurons in ALS eventually leads to their death. When the motor neurons die, the ability of the brain to initiate and control muscle movement is lost. With voluntary muscle action progressively affected, patients in the later stages of the disease may become totally paralyzed.
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Amyotrophic lateral sclerosis (ALS), AKA "Lou Gehrig's Disease," is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Motor neurons reach from the brain to the spinal cord and from the spinal cord to the muscles throughout the body. The progressive degeneration of the motor neurons in ALS eventually leads to their death. When the motor neurons die, the ability of the brain to initiate and control muscle movement is lost. With voluntary muscle action progressively affected, patients in the later stages of the disease may become totally paralyzed.
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Muscular dystrophy (MD) is a group of more than 30 inherited diseases. It causes weakening and breaking down of muscle fibres. The muscles become weak and susceptible to damage. This disease affects the voluntary or skeletal muscles, which control the movements of legs, arms, and trunk. It can also affect the heart muscles and other involuntary muscles, such as muscles in the gut. To know more visit here: www.lazoi.com
Duchenne muscular dystrophy is serious and the most common form of muscular dystrophy. It is invariably fatal. Until recently, there was little hope that the widespread muscle degeneration that accompanies this disease could be combated. Ayurvedic Rasayana treatment now offers that hope. Ayurvedic Rasayana molecules viz. Curcumin, Mamsagni, and Sukumar Guggul Rasayana are efficient to stop further deterioration of muscles due DMD. The medicines blocks nuclear k-factor and will help delay the muscle degeneration. Rasayana medicines do not alter the patient’s genetic code or introduce genetic materials into the body. These safe and natural medicines are developed and being clinically used by AMDS India for Care through Ayurveda research project since 1995. Questions & comments to Dr Mukesh D Jain mjainbhilai@gmail.com
A short presentation in Genetics about Duchenne Muscular Dystrophy. The presentation includes its signs, symptoms, the life expectancy of a patient, and its management.
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2. What is it? Muscular Dystrophy (MD) is a group of inherited diseases in which the voluntary muscles progressively weaken overtime. Heart and other organs can also be affected. MD affects more than 50,000 Americans. 9 major types: Duchenne, Myotonic, Becker, Limb-girdle, Facioscapulohumeral, Congenital, Oculopharyngeal, Distal, and Emery-Dreifuss
3. Can occur at any age Most common in young males. Type is based on what age the individual is when muscular dystrophy appears Also depends on how severe the disease is, which muscles it affects, rate of progression, and the way it appears. Some types of muscular dystrophy only affect males. Some individuals with this disease experience mild symptoms, while others suffer from severe muscle weakness, dying at an early age.
4. Causes Defects in certain genes The type of MD is determined by which gene is defective In 1986, researchers discovered the gene that, when defective causes Duchenne MD. In 1987, the muscle protein associated with this gene was given the name dystrophin When the gene fails to produce dystrophin, Duchenne MD occurs Duchenne muscular dystrophy is the most common and fatal childhood type.
5. Duchenne Muscular Dystrophy 1 in 3500 male births Begins with proximal muscle weakness around age 4 Progresses to distal muscles, making walking more difficult Around age 10, most children are in wheelchairs Some experience cognitive problems
6. Most types of MD are a form of inherited disease called X-linked disorders or genetic diseases that mothers can pass on to their child, even though the mothers are not affected by the disease. Some forms of MD are not inherited but occur because of a gene abnormality or mutation.
7. Symptoms All forms: muscle weakness Myotonic: muscle spasms or stiffening after use, hand weakness, foot drop Duchenne and Becker: clumsiness, frequent falling, difficulty getting up, waddling gait, curvature of the spine. Drooling, eyelid drooping
9. MD Diagnosis Muscle biopsy DNA testing Blood enzyme tests Electromyography or nerve conduction tests Electrodes are used to test the muscle and/or nerves
10. Treatment No cure Medications and therapy can relieve symptoms and slow progression of the disease However, scientists are researching ways to insert a working dystrophin gene into muscles of boys with Duchenne and Becker MD Also, researchers are exploring potential muscle-building drugs to help reverse progression Dietary supplements, creatine, and glutamine are other potential treatments being studied http://www.youtube.com/watch?v=JnDVRB1DIUA
11. Braces, wheelchairs, and canes can improve mobility Surgery on the spine or legs also may be an option to improve function. Exercise! People suffering from MD should be as active as possible. Physical inactivity may make the disease worse
12. Benefits of Exercise Primary focus is on gaining muscular strength and endurance Aerobic exercise is important in preventing excess body fat, as well as decreasing cardiovascular risk factors Stretching increases ROM and prevents contractures For children, exercise activities should be as game-like as possible
13. Medications Corticosteroids can slow muscle damage in patients with Duchenne muscular dystrophy. Phenytoin, procainamide, or quinine may treat delayed muscle relaxation for those with Myotonic MD. Medications can also be prescribed to treat heart problems in some forms of muscular dystrophy. Many studies are being conducted to find additional treatment methods
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15. References Durstine, J. Larry., and Geoffrey E. Moore. “Muscular Dystrophy." ACSM's Exercise Management for Persons with Chronic Diseases and Disabilities. 2nd ed. Champaign, IL: Human Kinetics, 2003. 254-258. "Muscular Dystrophy - PubMed Health." Web. 22 Mar. 2011. <http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0002172/>. "Muscular Dystrophy - Duchenne Muscular Dystrophy - Becker Muscular Dystrophy - Limb-girdle Muscular Dystrophy » Types of Muscular Dystrophy." Health, Fitness, Glamour Online Magazine. Web. 22 Mar. 2011. <http://www.magazine.ayurvediccure.com/types-of-muscular-dystrophy/>. www.webmd.com