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Examples include muscular dystrophy and myasthenia gravis. Obesity Excess fat; a body weight that is 30% more than the ideal body weight for a person’s height. Obsessive compulsive disorder A psychiatric (mental) disorder in which a person gets caught up in certain rituals, either thoughts or ways of doing things, that interfere with normal ...
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[DOC File]MUSCULAR DYSTROPHIES
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It is usually an adult onset disease that generally is onset by the age of 65. It is a progressive dementia disease ... Duchenne muscular dystrophy is due to a defect in the X-linked recessive gene. It is associated with generalized weakness and muscle wasting that affects the limb and trunk muscles in the beginning and then progresses to the ...
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[DOC File]National Institute of Neurological Disorders and Stroke ...
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X-Linked Muscular Dystrophy (Duchenne Muscular Dystrophy and Becker Muscular Dystrophy) ... Type Inheritance Locus Gene Clinicopathologic Features 1A Autosomal-dominant 5q31 Myotilin Onset in adult life with slow progression of limb weakness, but sparing of facial muscles; dysarthric speech 1B Autosomal-dominant 1q21 Lamin A/C Onset before the ...
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Includes muscular dystrophy (MD), myasthenia gravis, and amyotrophic lateral sclerosis (ALS), cerebral palsy (CP), reflex sympathetic dystrophy (RSD). Obesity The condition of …
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MUSCULAR DYSTROPHY. The muscular dystrophies are a group of inherited usually progressive muscular disorders of unknown cause. The age of onset, rate of progression, and cause of outcome are highly variable and depend on the type. Underwriting Requirements. An …
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Oct 12, 2014 · This dystrophy occurs worldwide but may be more common in Roma/Gypsye209,e216 and Tunisian populations.e208,e220 Onset occurred in the early childhood to adult years, but most series had an age at onset in early childhood, with a range of 1–13 years (mean 6.1 years) in one Class I studye208 and a range of 2–8 years in the other Class I ...
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List two symptoms of Duchenne’s muscular dystrophy. Describe the symptoms, treatment, and nursing care for the child with Legg-Calvé-Perthes disease. Objectives (cont.) Describe two topics of discussion applicable at discharge for the child with juvenile rheumatoid arthritis.
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Muscular Dystrophy Types & Causes of Each Form
Myotonic dystrophy (DM), a genetic and neuromuscular disorder, is the most common form of adult-onset muscular dystrophy resulting in symptoms such as proximal muscle weakness, myotonia, iridescent cataracts and cardiac arrhythmia. Myotonic dystrophy type 1 (DM1), the most prevalent type of DM, is caused by a (CTG)n expansion in the 3 ...
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Other forms of muscular dystrophy include oculopharyngeal muscular dystrophy (OPMD), distal muscular dystrophy, and Emery-Dreifuss muscular dystrophy. Currently, no treatment can stop or reverse the progression of any form of muscular dystrophy.
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[DOC File]Evidence-based Guideline: Diagnosis and Treatment of Limb ...
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Duchenne muscular dystrophy (DMD) is one of the types of muscular dystrophy, which is a group of genetic, degenerative diseases primarily affecting voluntary muscles. DMD is caused by an absence of dystrophin, a protein that helps keep muscle cells intact. Onset occurs during early childhood, about 2 …
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Adult onset muscular dystrophy types