Duchenne MD is the most common muscle dystrophy. Due to the way the disease is acquired, it generally influences young men. It is conceivable…
Duchenne muscular dystrophy has no cure, hence treatment focuses primarily on the underlying symptoms. Essentially, medical treatment includes administration of albuterol, amino acids, carnitine, coenzymes Q10, creatine, fish oil, green tea extracts, and vitamins. Other treatments to help minimize life-threatening conditions includes assisted ventilation, angiotensin-converting-enzyme inhibitors, beta-blockers, diuretics, proton pump inhibitors, and orthopedic appliances.…
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…
Duchenne muscular dystrophy (DMD) is a rare genetic disorder characterized by progressive muscle degeneration and weakness. DMD is caused by a mutation of a gene on the X chromosome that causes an absence of dystrophin, a protein that helps keep muscle cells intact. This very rare disease primarily affects young boys. Its symptoms include muscle weakness which can begin as early as the age of 3, first affecting the voluntary muscles such as the hips, pelvic area, thighs and shoulders, and by the early teens the involuntary muscles are affected such as the heart and lungs. There is no cure for this disorder. Boys affected by DMD did not survive beyond their teenage years until recently. Due to advances in cardiac and respiratory care, life…
Duchenne Muscular Dystrophy is caused by the lack of a protein called dystrophin and is fatal with the further developed symptoms. Without dystrophin the muscles expand, which makes it difficult to walk, sit, climb, stand, jump, and run. That is, the body makes no dystrophin for the muscles to be normal, and consequently a…
DMD is a degenerative neuromuscular disease caused by a defective gene related to the protein dystrophin (MDA, 2015, para. 1). Dystrophin is essential for maintaining the normal function of skeletal and cardiac muscles as it…
Mental illnesses are more readily labeled today than at any other time in history. Following this heightened awareness; substance abuse disorder has been established in the Diagnostic and Statistics Manual, 5th edition (DSM-5) as its own diagnostic category. The DSM-5 is a diagnostic tool employed by healthcare professionals in the procedure of determining the proper diagnosis as well as the course of treatment for individuals suffering from mental health disorders. Each year, thousands of people remain untreated as a result of their drug or alcohol use. Due to the stigma surrounding addiction, hesitation to fully disclose the substances that contribute to the symptoms experienced by a patient can cause a dual diagnosis to be difficult…
Muscular dystrophy (MD) is a group of nine neuromuscular diseases. This means it is related both to the nervous system and to the muscles. About 250,000 people in the United States have muscular dystrophy. Muscular dystrophy (MD) is a group of nine neuromuscular diseases. This means it is related both to the nervous system and to the muscles. About 250,000 people in the United States have muscular dystrophy. There are many different types of Muscular Dystrophy but how do they affect your body? Myotonic (also called MMD or Steinert's disease). The most common form of muscular dystrophy in adults, myotonic muscular dystrophy affects both men and women, and it usually appears any time from early childhood to adulthood. In rare cases, it appears in newborns (congenital MMD). The name refers to a symptom, myotonia -- prolonged spasm or stiffening of muscles after use. This symptom is usually worse in cold temperatures. The disease causes muscle weakness and also affects the central nervous system, heart, gastrointestinal tract, eyes, and hormone-producing glands. In most cases, daily living isn't restricted for many…
As you may know, Muscular Dystrophy is a disorder that weakens a person's muscle. More than 50,000 people are diagnosed with that kind of disorder. They usually come from the…
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.…
Parkinson's disease belongs to a group of conditions called movement disorders. Movement disorders describe a variety of abnormal body movements that have a neurological basis, and include such conditions as cerebral palsy, ataxia, and Tourette syndrome.…
Muscular Dystrophy, also referred to as “MD”, is a group of diseases that cause progressive weakness and loss of muscle mass (Mayo). In MD, abnormal genes interfere with the production of proteins needed to form the muscle’s health (Mayo). There are many long-term effects to this terrifying disease. The primary one, that being unable to walk. Muscular Dystrophy is a life-threatening disease that many pose questions and desire to learn more about.…
National Institute of Neurological Disorders and Stroke. “Restless Leg Syndrome Fact Sheet.” National Institute of Health. September 2010. Web. 31 March 2017. https://www.ninds.nih.gov/Disorders/Patient-Caregiver-Education/Fact-Sheets/Restless-Legs-Syndrome-Fact-Sheet. The National Institute of Neurological Disorders and Stroke (NINDS) is an Institute within National Institutes of Health. This article contains information about the sleeping disorder of restless leg syndrome. Restless leg syndrome is described as a neurological disorder that consists of painful feelings in the leg. The NINDS gives signs and symptoms that are commonly found in people who suffer from this disorder. Some symptoms of this disorder include feelings of pain, throbbing,…
A patient cannot be effectively treated if their diagnosis is incorrect. Sensory Processing Disorder is one of the top misdiagnosed mental disorders in children. The main contributor to the increasing misdiagnosis of SDP is classification system of mental illness used by medical providers (NCBI, 2009). There are more than 200 forms of mental illness (Triad Mental Health, 2015). Medical professionals use many criteria within a detailed system to evaluate and diagnose these disorders as well as categorize them. It is assumed that the system is perfect, however the psychological field of medicine has failed the majority of it patients (Science Based Medicine, 2012). Lines are often blurred between multiple diseases.…
Dysprosium (Dy), like any other natural element, is formed when a supernova occurs. A supernova is a rare celestial event wherein a dying star emits, in an extremely bright and short-lived manner, vast amounts of energy. When a supernova explosion occurs, elements heavier than iron are expelled out into space, eventually reaching Earth.…