Essay on Turner Syndrome - 1353 Words.
The Turner Syndrome (known as Ullrich-Turner Syndrome in Germany) is a congenital disease. A German doctor named Ullrich published his article in 1930. American doctor Henry Turner recognized a pattern of short stature and incomplete sexual maturation in otherwise normal females. He published a comprehensive medical description of the syndrome.
Gonadal Dysgenesis Gonadal Dysgenesis, also known as turner syndrome, is a rare medical disorder that affects 1 in every 2,500 girls (kidshealth). It is a chromosomal that occurs when one of the two X chromosomes found in females are missing or is incomplete. This condition only affects females.
Turner’s syndrome is a genetic condition in which a female does not have the usual pair of two X chromosomes. This medical disorder affects about 1 in every 2,500 girls. I do not know exactly what causes Turner syndrome, but researchers know that it is the result of a problem with a girl's chromosomes either not being there at all or only part of it is still there.
Turner Syndrome Introduction Turner Syndrome is a disorder that affects one in every two thousand girls. Usually girls are born with only one X chromosomes. Some are born with an extra chromosome, or sometimes even half of one is missing which causes Turner Syndrome.
Turner syndrome is a chromosomal condition, caused by deletion of all the second sex chromosomes or part of them. It is approximated that one in two thousand five hundred live female births is a turner syndrome patient. In pediatric practice, Turner syndrome is one of the most frequent conditions encountered in genetics.
Turner Syndrome is one of the rare diseases that affect only women. It is caused by abnormalities in one of the X-chromosomes, and has a number of symptoms, including short stature and the presence of a webbed neck. While Turner syndrome symptoms may be apparent at birth, the condition often isn't diagnosed until puberty.
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Turner Syndrome: A Chromosomal Disorder 1165 Words 5 Pages Turner Syndrome Shinji Lin December 15, 2015 Period 5 Turner syndrome is a chromosomal disorder that affects development in females. This condition is caused by a missing or incomplete X chromosome.
Turner’s Syndrome is a chromosomal condition, and, therefore, there is no cure for this genetic syndrome. However, much can only be done to help minimize the symptoms and effects of the syndrome, specifically in relation to the use of growth hormone and estrogen replacement therapy.
Turner syndrome can be diagnosed at any stage of life (“Turner Syndrome (a)”). It may be diagnosed before birth if chromosome analysis is done during prenatal testing. Unfortunately, there is no way to prevent Turner Syndrome, but there is care to help Turner syndrome patients live normal lives.
Turner’s syndrome is a genetic disorder that occurs in 1 in every 2,500 female births. Though it occurs in about 3% of fetuses, 99% of these fetuses are spontaneously aborted. Turner’s syndrome can be defined as a combination of phenotypes with varying expressivity along with the complete or partial loss of an X sex chromosome.
The Turner Syndrome (known as Ullrich-Turner Syndrome in Germany) is a inborn disease. A German physician named Ullrich published his article in 1930. American physician Henry Turner recognized a form of short stature and uncomplete sexual ripening in otherwise normal females. He published a comprehensive medical description of the syndrome.
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