Top-Rated Free Essay
Preview

Diseases of the Muscular System

Better Essays
1060 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Diseases of the Muscular System
Diseases of the Muscular System
There are over 650 muscles in the human muscular system. Each muscle has a specific role to perform. These muscles help us talk, walk, sit, run, eat, move about, hold things, and most important the continuous pumping of the heart muscles keeps us alive. Muscular system diseases cause many problems in the human body, that affects the mobility and functioning of various parts of the body. The list is very long as there are number of disorders that affect the human body.

Muscular Dystrophy
This is a genetic disease is a group of inherited muscle disease that causes damage to muscle fibers. The symptoms of muscular dystrophy disease include weakness, loss of mobility and lack of coordination. The most common diseases classified as muscular dystrophy are Duchenne, Becker, limb girdle, congenital, facioscapulohumeral, myotonic, oculopharyngeal, distal, and Emery-Dreifuss. The basic fact about muscular dystrophy is that there is no specific cure for muscular dystrophy.

Cerebral Palsy
Cerebral Palsy is one of the diseases that affects the muscular system, where a persons posture, balance and motor functions are affected. Brain damage during or before childbirth causes loss of muscle tone, causing problems carrying out physical tasks in children. It is one of the most common congenital disorders.

Fibrodysplasia Ossificans Progressiva
This is a very rare congenital disorder that causes the soft tissues to become hard like bones permanently. This causes the muscles, tendons, ligaments as well as other connective tissues to grow bones between the joints. Thus, leading to permanent restriction of movement. There is no effective Fibrodysplasia Ossificans Progressiva (FOP) treatment and pain is controlled using medications.

Dermatomyositis
The inflammatory myopathy that leads to chronic muscle and skin inflammation is called dermatomyositis. This is a progressive autoimmune disease of the connective tissues that causes muscle weakness. The dermatomyositis symptoms include muscle pain, hardened calcium deposits under the skin, gastrointestinal ulcers, intestinal perforations, lung problems, fever, fatigue and weight loss. It leads to a red or violet colored skin rash on the face, hands, knees, chest and back. There is no cure for this progressive muscle weakness but can be controlled using corticosteroids and immunosuppressive drugs.

Compartment Syndrome
Chronic compartment syndrome caused by compression of the blood vessels, nerves and muscles within a closed area of the body. This causes tissue death due to lack of oxygen. The compartment syndrome symptoms include severe muscle pain, feeling of tightness in muscles, paresthesia, paralysis, etc. Treatment involves immediate surgical treatment, called fasicotomy. This helps in relieving the pressure on the muscles and helping them become normal again.

Myasthenia Gravis
Myasthenia gravis is a chronic autoimmune disease characterized by muscle weakness and fatigue. There is a breakdown of the neuromuscular junction and thus, brain loses control over these muscles. The myasthenia gravis symptoms and signs include drooping eyelids, difficulty swallowing, muscle fatigue, breathing difficulty, inability to control facial expressions, etc. Medications and surgical intervention are a part of myasthenia gravis treatment.

Amyotrophic Lateral Sclerosis
Amyotrophic lateral sclerosis is a serious neurodegenerative disease. This disease is also known as the Lou Gehrig's disease. In this disease, the motor neurons destroy that leads to loss of control over voluntary muscle movement. The early symptoms of ALS include difficulty to swallow, breath and speak. Paralysis is an advanced Lou Gehrig's disease symptom.

Mitochondrial Myopathies
Mitochondrial myopathies is a condition where the mitochondria, the powerhouse of cells, is damaged. The symptoms of this neuromuscular disease include muscle weakness, heart rhythm abnormalities, deafness, blindness and heart failure. In some cases, it leads to seizures, dementia, drooping eyelids and vomiting. Other symptoms include breathing difficulty, nausea and headache.

Rhabdomyolysis
Rhabdomyolysis is a condition where there is rapid skeletal muscle destruction. This causes the muscle fibers to breakdown into myoglobin that is released into the urine. This leads to kidney failure as myoglobin is dangerous to the kidney. Rhabdomyolysis symptoms include muscle weakness, stiffness, and pain. If detected early, there is a possibility of rhabdomyolysis treatment. Treatment includes use of intravenous fluid, dialysis as well as hemofiltration in severe cases.
Polymyositis
Polymyositis is an inflammatory and degenerative muscular system disease. This is a systemic connective tissue disease that causes symmetric weakness and muscle atrophy to some extent.
Fibromyalgia
The debilitating, chronic muscle disorder is called fibromyalgia. It is characterized by pain, fatigue and many other symptoms like tenderness and stiffness of the muscles. It is seen affecting more women than men and is thought to be a genetic condition.

Myotonia
Myotonia is a condition where the muscles relax slowly after contraction and stimulation. The symptoms of myotonia include trouble while releasing a grip, walking and difficulty in getting up after sitting or sleeping. Medications, anticonvulsants and physical therapy is involved in treatment of myotonia.

Myofascial Pain Syndrome
Myofascial pain syndrome is a chronic muscle pain disorder. It is characterized by aches, pain and burning sensation around sensitive points of the muscles called the trigger points. One may also feel joint stiffness, area of tension like a knot and sleep problems due to severe pain. Use of corticosteroids, botulism toxin injections, massage therapy and physical therapy help in management of myofascial pain syndrome.

A Few Other Diseases of the Muscular System
There are a few other neuromuscular system diseases that may affect people. Some of these neuromuscular diseases are categorized according to their site of origin.

Congenital Muscular Diseases
Central core disease
Centronuclear myopathy
Congenital fiber type disproportion myopathy
Nemaline myopathy
Multominicore disease
Myotubular myopathy
Autophagic vacuolar myopathy
Zebra body myopathy
Cap disease
Hyaline body myopathy
Neuromuscular Junction Diseases
Lambert-Eaton Syndrome
Myasthenia Gravis
Piriformis Syndrome
Peripheral Nerve Diseases
Charcot-Marie Tooth Disease
DeJerine-Sottas Disease
Friedreich's Ataxis
Spinal Muscular Atropies
Infantile Progressive Spinal Muscular Atrophy
Intermediate Spinal Muscular Atrophy
Juvenile Spinal Muscular Atrophy
Adult Spinal Muscular Atrophy
Metabolic Diseases of the Muscular System
Acid Maltase Deficiency
Carnitine Palmityl Transferase Deficiency
Myoadenylate Deaminase Deficiency
Debrancher Enzyme Deficiency
Phosphoglycerate Kinase Deficiency
Rare Muscular System Diseases
Central Core Disease
Hyperthyroid Myopathy
Periodic Paralysis - Hypokalemic - Hyperkalemic
Myotubular Myopathy
Nemaline Myopathy
Myotonia Congenita
Paramyotonia Congenita
These were some of the diseases of the muscular system. These diseases can cause many debilitating conditions that reduce productivity and limit mobility. It is important to seek early medical help to control the diseases before the progress. Hope the above article has helped you learn all about the different disorders of the muscular system.

You May Also Find These Documents Helpful

  • Good Essays

    case study

    • 1194 Words
    • 4 Pages

    1. Dunchenne muscular dystrophy is a genetic disorder due to progressive weakness and degeneration of muscle cells over time, discovered by Guillaume Duchenne.…

    • 1194 Words
    • 4 Pages
    Good Essays
  • Satisfactory Essays

    Muscular System: The muscular systems is responsible for maintaining posture, circulating blood, and movement. Visceral muscle is found inside of organs like the stomach, intestines, and blood vessels. The stomach secretes acid and enzymes that digest food. The muscular system also has another variant which is skeletal muscle. The skeletal muscles are attached to bones and move various parts of the body. The biceps, pectoralis major, triceps, nasalis, and deltoid are five major organs in the muscular system. The biceps main job is to control the movement of the elbow and shoulder. The pectoralis major make up most of the chest bulk. The triceps help extend and retract the forearm. The nasalis compress nasal cartilage. The deltoid is responsible…

    • 128 Words
    • 1 Page
    Satisfactory Essays
  • Good Essays

    Muscular dystrophies are a group of genetic conditions characterized by progressive muscle weakness and wasting (atrophy). The Duchenne and Becker types of muscular dystrophy are two related conditions that primarily affect skeletal muscles, which are used for movement, and heart (cardiac) muscle. These forms of muscular dystrophy occur almost exclusively in males.…

    • 1511 Words
    • 6 Pages
    Good Essays
  • Good Essays

    Duchenne MD is the most common muscle dystrophy. Due to the way the disease is acquired, it generally influences young men. It is conceivable…

    • 884 Words
    • 4 Pages
    Good Essays
  • Satisfactory Essays

    Spinal muscular atrophy [SMA] is a disorder in which, you have a loss of motor neurons. Your muscle symmetry is often off. In addition, there is muscle weakness in your spinal cord. This occurs in a hard time sitting up and holding your head up on your own. It is just like when you are a newborn and you need a pillow to sit on the couch. A few major causes of SMA are loss of motor neuron cells or nerve cell. This mutation leads to a deficiency of motor neuron cells or nerve cells. The disorder SMA is tied to the gene "SMN1" and tied to chromosome 5. A few symptoms of this disorder are- difficulty breathing lack of oxygen, difficulty eating, floppy posture, small amount of movement, and all these symptoms will gradually get worse over time. All these symptoms are at about a mild level in the beginning.…

    • 417 Words
    • 2 Pages
    Satisfactory Essays
  • Better Essays

    Duchenne muscular dystrophy also known as DMD is a rare genetic condition that could affects all race and cultures; mostly boys. Duchenne muscular dystrophy affects 1 in 500 boys in approximation. According to muscular dystrophy association 20,000 children are born with DMD worldwide and approximately, 35% are as a result of spontaneous genetic mutation (2014). The disease is an X-linked recessive inheritance that the mother passed it on. DMD has a progressive muscular degeneration and weakness and it is one of the nine types of muscular…

    • 1130 Words
    • 5 Pages
    Better Essays
  • Good Essays

    Cerebral palsy is a condition in which permanent disabling symptoms are a result of damage to the motor control areas of the brain. Characteristics of cerebral palsy include abnormal reflex development, seizures, speech and language disorders, sensory impairments, bone growth, and respiratory conditions.…

    • 681 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Duchenne Muscular Dystrophy is a dangerous and rare disorder. It’s transferred through family generations because it’s a genetic disease. In addition, Duchenne Muscular Dystrophy is referred to by other names including DMD, Duchenne Syndrome, and Pseudohypertrophy. DMD is when the body cannot make dystrophin so it results in muscle weakness.…

    • 1141 Words
    • 5 Pages
    Good Essays
  • Good Essays

    Duchenne muscular dystrophy or DMD for short is a mutation that happens in the genes. Duchenne is mostly found in boys and rarely found in girls. Duchenne can be inherited in an x-linked fashion. The symptoms usually appear before the age of 6. Sometimes symptoms can start as early as infancy. Not all symptoms happen at one the first symptom is a usual delay of motor milestones such as using muscles to sit up, walk and stand alone. Calf muscles enlarge, this is also known as false enlargement. The enlarged calf muscle…

    • 1325 Words
    • 6 Pages
    Good Essays
  • Better Essays

    Duchenne Muscular Dystrophy is “an X-linked disease of muscle caused by an absence of the protein dystrophin” (Dr. Sussman). The disease affects young boys. If a boy…

    • 1398 Words
    • 6 Pages
    Better Essays
  • Good Essays

    Cumulative effects of wear and tear at the joint surface, or from genetic factors affecting collagen filaments.…

    • 1020 Words
    • 5 Pages
    Good Essays
  • Satisfactory Essays

    Muscular Dystrophy Essay

    • 446 Words
    • 2 Pages

    Muscular dystrophy (MD) is a group of genetic diseases involving progressive weakness and degeneration of the muscles that control movement. In some forms of MD, the heart muscles and other involuntary muscles, as well as other organs, are affected. There are 9 distinct types of MD.…

    • 446 Words
    • 2 Pages
    Satisfactory Essays
  • Better Essays

    What Is Cerebral Palsy?

    • 1527 Words
    • 7 Pages

    Cerebral Palsy is defined as a condition marked by impaired muscle coordination (spastic paralysis) and/or other disabilities, typically caused by damage to the brain before or at birth. Although Cerebral palsy is not contagious, a person can intentionally or unintentionally increase the possibility a child will develop Cerebral Palsy through abuse, medical malpractice, negligence, or the spread of a bacterial or viral infection (Stern, 2017). Cerebral palsy was first introduced in the mid 1800's by Dr. William John Little, whom suffered from several illnesses. He wrote the first medical descriptions, detailing a disorder that caused a spastic, stiff muscular disorder within children. Cerebral Palsy made it difficult for children to do simple…

    • 1527 Words
    • 7 Pages
    Better Essays
  • Better Essays

    Cerebral Palsy

    • 1154 Words
    • 5 Pages

    Cerebral Palsy (CP) is a condition that affects thousands of people each year. An estimated 764,000 children and adults are afflicted with one or more symptoms of CP. Around 8,000 infants and babies are diagnosed each year and 1,200-1,500 preschool age children are recognized with symptoms of CP (www.ucp.org). This condition is caused by “abnormal development of areas of the brain that control movement and posture” (www.ucp.org). It can also be caused by damage to the brain (usually because of head injury during the birthing process) or diseases/infections the mother has during pregnancy such as German measles, rubella, bacterial meningitis, or viral encephalitis. Other risk factors may be the loss of too much oxygen during birth and low birth weight.…

    • 1154 Words
    • 5 Pages
    Better Essays
  • Powerful Essays

    Cerebral Palsy

    • 1048 Words
    • 5 Pages

    Cerebral Palsy is a disorder of movement, muscle tone or posture. It affects the ability to move in a coordinated and purposeful way. The exact cause is unknown, but many cases are the result of problems during pregnancy in which the brain is damaged or it does not develop normally. It can be caused from anything that interferes with normal brain development such as infections and maternal health problems. It usually occurs before or during birth, or during the first 3 to 5 years of a child’s life. Cerebral palsy is one of the most common congenital (existing before birth or at birth) disorders of childhood.…

    • 1048 Words
    • 5 Pages
    Powerful Essays