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Turner syndrome is a genetic condition found in females only. It affects about 1 in every 2, girls. Girls who have this condition usually are shorter than average and infertile due to early loss of ovarian function. Usually, a person has 46 chromosomes in each cell, divided into 23 pairs, which includes two sex chromosomes. Half of the chromosomes are inherited from the father and the other half from the mother. The chromosomes contain genes, which determine an individual's characteristics, such as eye color and height.
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Turner Syndrome (for Teens) - MedStar Health
Turner Syndrome "Its a Girl Thing". What is Turner Syndrome? This unique absence of an X chromosome therefore results in various physical features that differ greatly from the average standard human who has not obtained the defect. Turner Syndrome had several implications on the physical and mental aspect of the Human body and mind. Further results indicated specific impairments in visuospatial and memory areas and significant underachievement in arithmetic, particularly numerical ability, mental calculation, geometry, and reasoning. Figure 1. The diagram reveals the swelling and inflammation that are the physical traits that are associated with Lymphedema.
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Turner syndrome TS is a genetic condition found in females only. It affects about 1 in every 2, girls. Girls with Turner syndrome are usually shorter than their peers. The good news is that if TS is diagnosed while a girl is still growing, she can be treated with growth hormones to help her grow taller.
Back to Health A to Z. Turner syndrome is a female-only genetic disorder that affects about 1 in every 2, baby girls. This chromosome variation happens randomly when the baby is conceived in the womb. It isn't linked to the mother's age. Read more about the genetic cause of Turner syndrome.