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Most disorders of chromosome number that occur in humans causes symptoms so severe that the developing fetus dies, often before the woman even relizes she is pregnant. Fortunately, these disorders occur rarely. However Down syndrome is the only autosomal trisomy in which the affected individual lives into adulthood. It occurs in about one in every 700 live births,

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What is the disorder caused by having an abnormality on chromosome 21?

Down's Syndrome or trisomy 21.


Trisomy is a mutation that results in a cell having an extra?

A trisomy is a condition in which a person has three copies of a chromosome instead of the usual two copies. A person can have full trisomy (three copies in every cell) or mosaic trisomy (three copies in some cells but not all).


Which genetic disorder does an extra chromosome cause?

An extra chromosome can cause genetic disorders such as Down syndrome, which is caused by an extra copy of chromosome 21. This leads to developmental delays, intellectual disabilities, and certain physical characteristics.


What condition occurs when a human zygote has 47 chromosomes?

A human zygote with 47 chromosomes has a condition called trisomy, specifically trisomy 21 if the extra chromosome is chromosome 21. This results in Down syndrome, a genetic disorder characterized by intellectual disability and physical abnormalities.


Trisomy-21 results from a mutation to the chromosomes in?

Trisomy-21, also known as Down syndrome, results from an extra copy of chromosome 21. Instead of the usual two copies, individuals with Down syndrome have three copies of chromosome 21. This extra genetic material can lead to various physical and cognitive differences.


What is trisomy mutation?

A trisomy is when a person has 3 versions of a chromosome. 'Normal' humans will only have 2 of each chromosome. For example, having 3 versions of chromosome 21 is known as Trisomy 21 or Down Syndrome.


Which condition results when cells receive three copies of chromosomes 21?

Down syndrome results when cells receive three copies of chromosome 21.


How does nondisjunction cause Trisomy 21?

Nondisjunction is a process during cell division where chromosomes fail to separate correctly. In Trisomy 21, an individual has three copies of chromosome 21 instead of the usual two, which is caused by nondisjunction during either meiosis I or meiosis II in the formation of gametes. When a gamete with an extra copy of chromosome 21 is fertilized, it results in an individual with Down syndrome.


What is the relationship between trisomy 21 and Down syndrome?

Trisomy 21 is down's syndrome, which is an extra copy of chromosome 21


What would trisomy 21 look like in a karyotype?

The trisomy 21 in a karyotype would look like extra chromosome 21 I ^^


What trisomy causes Down syndrome?

Well, honey, Down syndrome is caused by an extra copy of chromosome 21, also known as trisomy 21. It's like having a bonus chromosome that messes with the genetic party. So, to put it simply, trisomy 21 is the culprit behind Down syndrome.


What is the presence of three of a particular chromosome?

The presence of three copies of a particular chromosome is known as trisomy. This genetic condition can lead to developmental abnormalities, such as Down syndrome which is caused by trisomy of chromosome 21.