It is indeed hard to convince people that human genetic disorders often result from unbalanced chromosomes abnormalities where there is a gross loss or rather gain of a genetic material. Apparently, various complex phenotypes in the body are attributed to this genetic imbalance where it disrupts dosage-sensitivity as well as the development of important genes. This paper intends to discuss Duchenne muscular dystrophy genetic disorder as well as the related impact on a particular victim.
Question #1
One of the most common disorders associated to chromosomes imbalance is the Duchenne muscular dystrophy (DMD) and is often characterized by progressive muscles degeneration as well as the weakness (Abu-Hussein, Watted, Yehia, Proff, & Iraqi, 2015). While there have been various researches concerning the cause of DMD, lack of dystrophin is regarded as the main cause of such disorder. Primarily, dystrophin is a type of proteins that aid the body in keeping the muscle cells intact. While most of its symptoms are noticed at an early childhood, its effect on a patient is immense.
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