What causes Klinefelter syndrome meiosis?

Does Klinefelter’s occur in meiosis 1 or 2?

The most frequent chromosomal complement associated with Klinefelter syndrome is 47,XXY, which may result from a nondisjunction during (1) meiosis I or meiosis II of oogenesis, or (2) meiosis I of spermatogenesis.

How is Klinefelter syndrome caused?

Klinefelter syndrome is caused by an additional X chromosome. This chromosome carries extra copies of genes, which interfere with the development of the testicles and mean they produce less testosterone (male sex hormone) than usual.

Why can XXY only occur in meiosis 1?

Klinefelter’s syndrome, XXY males, can occur due to nondisjunction of X chromosomes during prophase of meiosis I in females. One of the eggs from such a meiosis could receive both X chromosomes, and the other would receive no X chromosomes.

Can a girl have Klinefelter’s syndrome?

Klinefelter syndrome affects males only; females cannot have it. Klinefelter syndrome results from a genetic abnormality in which males have an extra copy of the X chromosome. Instead of the usual XY chromosomes, males with Klinefelter syndrome have an XXY pattern.

Who is most likely to get Klinefelter’s syndrome?

Klinefelter syndrome occurs in about 1 out of 500 to 1,000 baby boys. Women who get pregnant after age 35 are slightly more likely to have a boy with this syndrome than younger women.

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Why are Klinefelter males tall?

From early school age, boys with Klinefelter’s syndrome tend to be taller (increased leg length) because testosterone normally stops boys growing after puberty. This increase in height is maintained throughout life. Patients with Klinefelter’s syndrome may have reduced coordination compared with other boys.

Is Klinefelter syndrome caused by Nondisjunction?

The 47,XXY karyotype of Klinefelter syndrome spontaneously arises when paired X chromosomes fail to separate (nondisjunction in stage I or II of meiosis, during oogenesis or spermatogenesis). Maternal and paternal meiotic nondisjunction each account for approximately 50% of Klinefelter syndrome cases.

Is Klinefelter syndrome autosomal or Sexlinked?

Klinefelter syndrome with fabry disease–a case of nondisjunction of the X-chromosome with sex-linked recessive mutation.

What is a fractured chromosome?

Description: Chromosome breakage disorders are a group of related diseases which are characterized by spontaneous chromosome breakage, immunodeficiency and predisposition to malignancy. These conditions include Fanconi Anemia, Ataxia-Telangiectasia, Bloom syndrome, LIG4 syndrome, and Nijmegen breakage syndrome.