Marfan syndrome is a heritable condition that acts the alignment tissue. The primary purpose of connective tissue is to hold the organic structure together and provide a framework for growth and development.
. In Marfan syndrome, the connective tissue is defective and does non act as it should. Because connective tissue is assemble throughout the body, Marfan syndrome can affect many body systems, including the skeleton, eyes, heart and blood vessels, nervous system, skin, and lungs. Marfan syndrome affects men, women, and children, and has been found among people of all races and ethnic backgrounds. It is estimated that at least 1 in 5,000 people in the United States have the disorder.
good deal can inherit Marfan syndrome, meaning that they get the mutation from a parent who has the disorder.
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This is the case in about 3 out of 4 people with Marfan syndrome. Other people have a spontaneous mutation, meaning that they are the first in their family to have Marfan syndrome. great deal with Marfan syndrome have a 50-50 chance of passing the mutation on each time they have a child. People are born with Marfan syndrome but may not key any features until later in life. Marfan syndrome features can appear at any age, including in infants and young children. They may get worsened as people age. Although everyone with Marfan syndrome has a defect in the aforementioned(prenominal) gene, different mutations are found in different families, and not everyone experiences the same characteristics to the same degree. In other...If you want to get a full essay, order it on our website: Orderessay
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