Klinefelter syndrome is not typically lethal; most individuals with the condition lead healthy lives. It is a genetic disorder caused by the presence of an extra X chromosome in males, leading to various physical and developmental challenges, but it does not usually result in mortality. With appropriate medical care and support, individuals with Klinefelter syndrome can manage symptoms and improve their quality of life.
People with Klinefelter's syndrome are not hermaphrodites, and people who are hermaphrodites do not have Klinefelter's syndrome.
The only genotype to cause Klinefelter's syndrome is XXY.
Mr. Klinefelter
Klinefelter's syndrome was first identified in 1942 by Harry Klinefelter and his colleagues. They described a group of men with underdeveloped testes and other characteristic features that became known as Klinefelter's syndrome.
there are five base pairs in klinefelter syndrome
what is kinefelter syndrome?
Klinefelter's syndrome is not considered to be a variation of normal, so by definition it is abnormal.
About 1/1000 to 1/500 males have Klinefelter's syndrome.
The genotype for a person suffering with Klinefelter's syndrome is XXY.
No, Klinefelter syndrome and Turner syndrome are the result of nondisjunction of sex chromosomes. Klinefelter syndrome is caused by an extra X chromosome (XXY), while Turner syndrome is due to a missing X chromosome (XO).
The parents have normal genotypes, because Klinefelter's syndrome is not inherited.
All people with Klinefelter's syndrome are male because by definition Klinefelter's syndrome is due to a genotype of XXY. The fetus will develop into a male if there are any Ys present at the sex chromosome.