No, only the gametes would be indicative of sterility. It is possible that the individual (though incredibly rare) to have "chimera" syndrome, where two non-identical twins merge to form one fetus. Turner's Syndrome is the absence of the male sex chromosome BTW. That chromosome carries little genetic information, and is possible during mitosis to "loose" it, but still create a mostly viable cell.
There are 3 types of Turner syndrome Classic Turner syndrome - 45X - second X chromosome missing from all cells. Mosaic Turner syndrome - 45X/46XX - second X chromosome missing from some cells. The third type of Turner syndrome is when the second X chromosome is damaged or only partly missing.
Turner syndrome is caused by a missing or incomplete X chromosome in females. It is typically not inherited, but rather occurs as a random event during the formation of reproductive cells in one of the parents. It is not passed down from parent to child.
Hyperplasia affects the all types of muscle cells.
Depending on the type of Turner syndrome a person has, their karyotype is either: 45X - classic Turner syndrome - second X chromosome missing from all cells 45X/46XX - Mosaic Turner syndrome - second X chromosome missing from some cells. There is another type of Turner syndrome, but it has a more complicated karyotype and I am not sure what the karyotype is off the top of my head.
Individuals with Turner syndrome typically have a genotype of 45,X, meaning they only have one X chromosome instead of the usual two. This genetic condition affects women and is associated with various physical and developmental differences.
There are 3 types of Turner syndrome Classic Turner syndrome - 45X - second X chromosome missing from all cells. Mosaic Turner syndrome - 45X/46XX - second X chromosome missing from some cells. The third type of Turner syndrome is when the second X chromosome is damaged or only partly missing.
Turner Syndrome is a genetic disorder that affects females only. It is caused by the absence of all or part of one of the X chromosomes. This condition is not passed down through family genetics, but occurs randomly.
Turner syndrome is caused by a missing or incomplete X chromosome in females. It is typically not inherited, but rather occurs as a random event during the formation of reproductive cells in one of the parents. It is not passed down from parent to child.
Turner syndrome is the result of one of the two X chromosomes being missing or damaged in some or all cells. These chromosomes are the sex chromosomes, which determine whether a person will be male or female. As people with Turners only have an X chromosome and no Y chromosome they are born female.
If a person is diagnosed in adolescence, depending on their age the doctor does a bone age x-ray to determine whether growth hormone is worth considering. The treatment for all adolescents and women with Turner syndrome is hormone replacement therapy.
No. Marfan syndrome is found equally across all ethnicities and genders.
No, down syndrome is caused by a genetic defect where there is an extra chromosome in most,if not all, of the cells of a body. it is not caused by a drug.
Hyperplasia affects the all types of muscle cells.
The same as all of the other cells.
Depending on the type of Turner syndrome a person has, their karyotype is either: 45X - classic Turner syndrome - second X chromosome missing from all cells 45X/46XX - Mosaic Turner syndrome - second X chromosome missing from some cells. There is another type of Turner syndrome, but it has a more complicated karyotype and I am not sure what the karyotype is off the top of my head.
Individuals with Turner syndrome typically have a genotype of 45,X, meaning they only have one X chromosome instead of the usual two. This genetic condition affects women and is associated with various physical and developmental differences.
Yes! It is in every body cell.