No it is caused by the Non-Disjunction of sex Chromosomes. Males with Klinefelter's syndrome have an extra X chromosome.
Mutation of a gene is not necessary for Klinefelter's Syndrome. It is an autosomal disorder meaning that an entire chromosome failed to disjunction during anaphase and so there are 2 X chromosomes and a Y chromosome.
Klinefelter's syndrome is not a mutation; rather, it is a chromosomal condition caused by the presence of an extra X chromosome in males, typically resulting in a 47,XXY karyotype. This additional chromosome disrupts normal development, leading to various physical and developmental characteristics. It occurs during the formation of reproductive cells or in early fetal development, rather than being a mutation in a specific gene.
Klinefelters syndrome occurs in a male and it is when they carry and extra X chromosome having a total of 47chromosomes rather than the usual 46. Thus resulting in a chromosomal mutation.
Mr. Klinefelter
Mr. Klinefelter
People with Klinefelter's syndrome are not hermaphrodites, and people who are hermaphrodites do not have Klinefelter's syndrome.
Zach Klinefelter's birth name is Zachary William Klinefelter.
Klinefelter's syndrome is typically caused by the presence of an extra X chromosome in males (XXY). It usually occurs as a result of a random error in cell division during the formation of sperm or egg cells. It is not inherited from parents.
Zach Klinefelter is 5' 7".
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.
The only genotype to cause Klinefelter's syndrome is XXY.