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Is the William syndrome a mutation?

Yes, Williams syndrome is a genetic condition caused by a deletion of genetic material on chromosome 7. This deletion is not usually inherited, but occurs randomly. It is not considered a mutation in the traditional sense, but rather a genetic anomaly.


How long does stickler syndrome last?

Stickler syndrome is a genetic disorder that is present from birth and persists throughout a person's life. The symptoms and severity of the condition can vary widely among individuals, but the genetic mutation that causes Stickler syndrome is lifelong. Treatment is focused on managing symptoms and complications associated with the syndrome.


Is Down syndrome considered a neurological disorder?

Yes, Down syndrome is considered a genetic disorder that affects the neurological development of individuals.


What are the key differences between Klinefelter syndrome and Turner syndrome?

Klinefelter syndrome is a genetic condition in males where they have an extra X chromosome, resulting in symptoms like infertility and low testosterone levels. Turner syndrome, on the other hand, is a genetic condition in females where they are missing part or all of one of their X chromosomes, leading to symptoms like short stature and infertility.


What are the key differences between Turner syndrome and Klinefelter syndrome?

Turner syndrome is a genetic condition in females where one of the X chromosomes is partially or completely missing, leading to short stature, infertility, and other physical characteristics. Klinefelter syndrome is a genetic condition in males where there is an extra X chromosome, resulting in infertility, low testosterone levels, and other physical characteristics.