Muscular Dystrophy And The Mda

“It makes life very hard,” says 18-year old Zachary Kolwyck. “I was never commensurate to compete in sports like my friends, I was always thrown out in baseball, and I couldn’t keep up during soccer. There are days when it’s hard for me to near get out of bed in the morning”. Zachary was diagnosed with Becker’s muscular dystrophy at the young age of three. Since then, every(prenominal) day has been a challenge, and he knows life is only liberation to become more difficult. Zachary is not alone. Statistics shoe that over 250,000 Americans are affected by some form of muscular dystrophy.
harmonise to the MDA website, there are nine types of muscular dystrophy. The two prominent forms are Becker muscular dystrophy, and Duchenne muscular dystrophy. Becker muscular dystrophy is the least(prenominal) severe form of muscular dystrophy; it causes weakness in the muscles of the hips, legs and pelvis. While Becker muscular dystrophy can be diagnosed during childhood, umpteen individuals who are affected are not diagnosed until their teenage years. Children affected by Becker muscular dystrophy can be evaluate to survive into mid- to late adulthood. On the opposite end of the spectrum, children nutrition with DMD are usually not expected to live ago their thirties.



Duchenne muscular dystrophy causes weakness in all the unpaid muscles, and affects the breathing muscles and the heart.
Muscular dystrophy is an X-linked recessive gene. It is carried by the mother, though no symptoms of the disease are present. It is then passed from the mother to her offspring, and normally is present in her male children. Rarely, muscular dystrophy is seen in female children, though when a female is affected, she is most practically a carrier. Muscular dystrophy is caused by either the light production or the absence of the protein that keeps muscle cells intact, called dystrophin. The dystrophin gene is a large gene comprised of 97 exons (a gene in a DNA sequence that...If you want to get a adept essay, order it on our website: Orderessay



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