A Speech on Living and Thriving with Merosin Deficient Congenital Muscular Dystrophy
Hello everyone! My name is Hannah. Today I am going to share with you some things that make me unique and to help you get to know me better. The goal I’m currently working on is to receive a bachelor '5 degree in history. From a young age, I have found ancient civilizations to be very fascinating. Ancient Egypt is my favorite period of history to study. After college. I plan on being either an archeologist or a college professor…...
DisabilityHealthHealth CareMuscular Dystrophy
An Introduction to Duchenne’s Muscular Dystrophy as a Result of a Defective Gene on the X Chromosome
Duchenne's muscular dystrophy is the result of a defective gene on the X chromosome. This gene is responsible for production of the muscle protein dystrophin. Dystrophin is an integral pan of the dystrophin-glycoprotein complex which bears the brunt of the force generated during muscular contraction. When dystrophin is not produced, the dystrophin»glycoprotein complex (DCG) is not present. Absence of the DCG leads to tears in the muscle membrane because the muscle membrane bears the force of muscular contraction alone. Tears…...
AnatomyBiologyBiotechnologyMuscular Dystrophy
The Features of the Muscular Dystrophy Diseases
Genetic diseases are inherited disorders reflecting gene mutations or abnormalities in chromosome structure or number and resulting in functional or anatomical changes. The frequency of chromosome abnormalities in the United States is 1 in about 200 live births. Approximately 5060 percent of all recognized spontaneous abortions are chromosomally abnormal. Six in every 100 stillbirths have chromosome abnormalities. and 6 in every 100 neonatal deaths are associated With chromosome defects (www.geneticalliance.org). Gene transmission, or heredity, in families is most often identified…...
DiseaseHealthMedicineMuscular Dystrophy
Characteristics of Duchenne Muscular Dystrophy, a Rare Inherited Neuromuscular Disorder
Genetic diseases are inherited disorders reflecting gene mutations or abnormalities In chromosome structure or number and resulting in functional or anatomical changes. The frequency of chromosome abnormalities in the United States is 1 in about 200 live births. Approximately 5060 percent of all recognized spontaneous abortions are chromosomally abnormal. Six in every 100 stillbirths have chromosome abnormalities. and 6 in every 100 neonatal deaths are associated with chromosome defects. Gene transmission, or heredity, in families is most often identified by…...
HealthMedicineMuscular Dystrophy
Topic of the Duchenne Muscular Dystrophy
Duchenne Muscular Dystrophy is one of the twenty known types of Muscular Dystrophy Diseases. Also called DMD, this disease is one of forty neuro-muscular diseases that changes lives daily. This disease is the most common childhood disease out of all of the neuro-muscular diseases, affecting one in every 3,500 boys in the world. The outcome of DMD is usually inevrtable, a result of death before the age of 25. However, the receivable information, increasing medical advances. and growing support for…...
HealthMedicineMuscular Dystrophy
Do You Have Muscular Dystrophy Enough Dystrophin?
Muscular dystrophy is a disorder that causes muscle decline, muscle contractions, and movement impairment. The disorder is often identified through heart and respiratory problems as well, which are effects that may prove fatal. In particular, Duchenne muscular dystrophy is caused by lack of a protein called dystrophin in muscles. Dystrophin is an essential part of a protein complex in muscles, so its absence affects muscle function. Current research indicates that most cases of Duchenne muscular dystrophy are due to genetic…...
EpidemiologyHealthMedicineMuscular Dystrophy
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