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Nondisjunction, the failure of chromosomes to separate properly during cell division, can lead to genetic disorders, such as Down syndrome or Turner syndrome, which are often associated with health challenges. However, not all instances of nondisjunction result in severe consequences; some individuals may experience mild symptoms or be asymptomatic. Additionally, nondisjunction can contribute to genetic diversity and evolution over long periods, highlighting that its effects can be context-dependent.

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Nondisjunction can alter the number of chromosome as well as autosomes?

Nondisjunction is a genetic error during cell division that can result in an abnormal number of chromosomes, affecting both autosomes and sex chromosomes. This can lead to conditions such as Down syndrome, Turner syndrome, or Klinefelter syndrome, depending on which chromosomes are affected.


The faillure of chromosomes to separate during meiosis is called?

The failure of chromosomes to separate during meiosis is called nondisjunction. This can result in an incorrect number of chromosomes in the daughter cells, leading to genetic disorders such as Down syndrome.


What are the three types of nondisjunction?

The three types of nondisjunction are autosomal nondisjunction, sex chromosome nondisjunction, and structural chromosome nondisjunction. Autosomal nondisjunction involves the failure of homologous chromosomes to separate during cell division. Sex chromosome nondisjunction involves the failure of sex chromosomes to separate. Structural chromosome nondisjunction involves the incorrect separation of chromosome parts during cell division.


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How is nondisjunction inherited?

Nondisjunction is an error in cell division that can lead to an abnormal number of chromosomes in a cell. When nondisjunction occurs in germ cells, it can be inherited by offspring, leading to genetic disorders such as Down syndrome. The risk of inheriting nondisjunction increases with parental age.


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