0
What else can I help you with?
When was Klinefelter's syndrome discovered?
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.
How prevalent is the klinefelter syndrome in the population?
About 1/1000 to 1/500 males have Klinefelter's syndrome.
Are klinefelter syndrome and Turner syndrome results of nondisjunction of autosomes?
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).
What is the sex of an offspring with kinefelters syndrome?
An individual with Klinefelter syndrome is male. They are born with at least one extra X chromosome (XXY), which can affect their physical and cognitive development.
Which chromosome Klinefleter's Syndrome affect?
Klinefelter Syndrome is neither recessive or dominant. It is a chormosome disorder, and is thus not passed down from generation to generation. The disorder is a random even that occurs.
Does a hermaphrodite have klinefelter?
People with Klinefelter's syndrome are not hermaphrodites, and people who are hermaphrodites do not have Klinefelter's syndrome.
Does klinefelters syndrome affect women?
Klinefelter syndrome primarily affects males, as it is caused by the presence of an extra X chromosome in males (typically resulting in a 47,XXY karyotype). Women do not have this chromosomal configuration, so Klinefelter syndrome does not directly affect them. However, women may experience related genetic conditions or variations, but these are not classified as Klinefelter syndrome.
What genotypes cause Klinefelter's syndrome?
The only genotype to cause Klinefelter's syndrome is XXY.
Who discover klinefelter syndrome?
Mr. Klinefelter
When was Klinefelter's syndrome discovered?
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.
How many base pairs are in Klinefelter's syndrome?
there are five base pairs in klinefelter syndrome
Klinefelter syndrome is what?
what is kinefelter syndrome?
Is klinefelter's syndrome a abnormality?
Klinefelter's syndrome is not considered to be a variation of normal, so by definition it is abnormal.
How prevalent is the klinefelter syndrome in the population?
About 1/1000 to 1/500 males have Klinefelter's syndrome.
Which could be the genotype for a male suffering from Klinefelter's syndrome?
The genotype for a person suffering with Klinefelter's syndrome is XXY.
Are klinefelter syndrome and Turner syndrome results of nondisjunction of autosomes?
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).
What are the genotypes of two parents that pass on the klinefelter's syndrome?
The parents have normal genotypes, because Klinefelter's syndrome is not inherited.
