Duchenne Muscular Dystrophy Essay

X-Linked Inheritence The topic which is assogned to me is X- linked inhertance that is a pattern of inheritance in which the spread of traits differentiate according to the sex of the individual because the genes which are present on the X chromosome have no counterparts on the Y chromosome. The inheritance pattern can be recessive or dominant. The trait firm by a gene on the X chromosome is always expressed in males.Because we know that males only d have one X chrmosome whichever the disease related

Muscular Dystrophy and Its Effect on the Body System Muscular Dystrophy also known as MD, is made up of a group of genetic diseases where muscle fibers are unusually susceptible to damage and the damaged muscles become progressively weak. Muscular Dystrophy is caused by certain defects with a specific type of gene known as the abnormal gene. Majority of muscular dystrophies come from an inherited disease referred to as X-linked disorders or genetic diseases in which mothers can transmit to their

Muscular dystrophy is a group of diseases that cause an abnormal progressive deteriorating of the muscles, leading to muscle weakness. Many different types of dystrophy are known, characterized by the muscle groups affected. The disease is caused from a genetic mutation that prevents a protein essential for normal muscle activity from being made, or being produced correctly. In each type of muscular dystrophy, a different protein is irregular (Emery, 2008). Furthermore, because this disease is due

The coexistence of the uncommon disease known as Duchenne Muscular Dystrophy or DMD, has come to the attention of many and has manifested within this document to generalize the history, impact, and significance of the disease. The history of DMD stemmed from the progressive muscular dystrophy of two 10-year-old boys names Conte and Gonji in 1836. Since this becoming the first historical account of such a disease, many doctors and specialists speculated a more catastrophic form of tuberculosis; when

Collaborative Learning Community: MD IEP Grand Canyon University Duchenne Muscular Dystrophy The Individual Educational Plan (IEP) is the driving document that promotes academic success. It is important when designing the Individual Educational Plan that the annual goals are determined based on the team analyzing the disability

OTH604 DIAGNOSIS FACT SHEET Muscular Dystrophy DIAGNOSIS: Muscular Dystrophy is a group of diseases that cause progressive weakness and loss of muscle mass. DESCRIPTION: • X- Linked recessive pattern passed on by mother to son • Nine major forms of muscular dystrophy: o Myotonic: most common form of muscular dystrophy in adults. Usually appears any time from early childhood to adulthood.) o Duchenne: affects only males, appears between the ages of 2 and 6. o Becker :symptoms appear later

Description of Muscular Dystrophy. The first record of Muscular Dystrophy (MD) was reported in 1830 by Sir Charles Bell when he wrote a paper about the disease. Symptoms of Muscular Dystrophy: •Difficulty getting up from a lying or sitting position •Walking on the toes •Learning disabilities •Large calf muscles •Frequent falls •Trouble running and jumping All of the symptoms of Muscular Dystrophy are found in males but women can carry the gene but most women aren't affected by it

Abstract Introduction 1.1 Muscular Dystrophy The genetic disease known as Muscular Dystrophy first appeared in history in the year 1830. It was included in a written report by the Scottish Neurologist Sir Charles Bell. The disease soon became more prominent, where it appeared in several medical journals from the 1850’s and onwards. Several young boys were described as having a weakness which progressively worsened, along with problems walking. The disease led to their eventual premature deaths.

Becker muscular dystrophy is a degenerative muscular disorder mainly affecting the voluntary muscles. This disease was named after the doctor who discovered it in the 1950s. BMD as it is called, affects the heart but not a severely as Duchenne muscular dystrophy. The symptoms of BMD usually start to affect the person during late childhood and adolescence. The first symptoms start with weakness in the legs and pelvis area , as well as the shoulders. It also affects the heart as the myocardium layer

Muscular Dystrophy: Roots, Cause, and Current Research Muscular dystrophy is an inherited disease that was discovered in 1861, by Guillaume B.A. Duchenne. Muscular dystrophy is a group of heredity disorders characterized by rapidly-worsening muscle weakness. The trait for muscular dystrophy may be transmitted as an autosomal dominant which means a disorder that has two copies of an abnormal gene that must be present in order for the disease or trait to develop. In this case, if some original