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Yes, it is a chromosomal error which occured most likely during meiosis. It is an error in cell division called NONDISJUNCTION. The single X chromsome is maternal, which suggests that the meiotic error tends to be paternal (3/4 of cases)

-Krista D. RN

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What is the mode of inheritance of turner's syndrome?

Turner syndrome is typically the result of a random event, rather than being inherited from a person's parents. It is caused by a complete or partial absence of one of the X chromosomes, leading to a variety of physical and developmental differences.


What are some chromosomal disorders?

The most common type of chromosomal disorder is the Down syndrome caused by an added copy of chromosomes 21. More common chromosomal disorders are Klinefelter's syndrome and Turnerâ??s syndrome.


What are the scenarios of passing turner syndrome?

Turner syndrome is a genetic condition that affects females, typically resulting in short stature, delayed puberty, and infertility. Some individuals may also experience heart defects, kidney abnormalities, and learning disabilities. Although it is a lifelong condition, many individuals with Turner syndrome lead healthy and fulfilling lives with medical monitoring and support.


What type of disorders are karyotyping used to diagnose?

Chromosomal disorders can be observed in a human karyotype. It can show whether there are extra chromosomes, or missing chromosomes, or malformed chromosomes, or whether chromosomes have extra pieces, or missing pieces.


What information can be obtained about a fetus from a karyotype?

A karyotype can provide information about the number, size, and shape of an individual's chromosomes. This can help detect chromosomal abnormalities such as Down syndrome or Turner syndrome in a fetus.

Related Questions

What is the method of transport for the turner syndrome?

Turner syndrome cannot be transported from one person to another as it is a chromosomal disorder.


What are the 3 major chromosomal disorders?

The three major chromosomal disorders are Down syndrome, Turner syndrome, and Klinefelter syndrome. Down syndrome is characterized by an extra copy of chromosome 21, Turner syndrome involves a missing or incomplete X chromosome in females, and Klinefelter syndrome is caused by an extra X chromosome in males.


What chromosomal abnormality causes Turner syndrome?

If one of sex chromosomes is missing. Normal-XX Turner- XO


What is the mode of inheritance of turner's syndrome?

Turner syndrome is typically the result of a random event, rather than being inherited from a person's parents. It is caused by a complete or partial absence of one of the X chromosomes, leading to a variety of physical and developmental differences.


What are some chromosomal disorders?

The most common type of chromosomal disorder is the Down syndrome caused by an added copy of chromosomes 21. More common chromosomal disorders are Klinefelter's syndrome and Turnerâ??s syndrome.


How can you get turner syndrome?

You can't catch it, it's a chromosomal disorder meaning you only have 1 X chromosome.


Can you get Turner syndrome?

You can't catch it, it's a chromosomal disorder meaning you only have 1 X chromosome.


This type of error is known as and usually results in zygotes that either do not develop to term or have severe abnormalities.?

This type of error is known as a chromosomal abnormality, which can occur during cell division and lead to an incorrect number of chromosomes in the zygote. Such abnormalities often result in zygotes that either fail to develop to term or develop severe congenital defects. Common examples include conditions like Down syndrome, Turner syndrome, and Klinefelter syndrome, which can arise from these chromosomal issues.


Is turner syndrome inheritable or random?

Turner syndrome is usually random and not inherited. It occurs when a female is born with a missing or incomplete X chromosome. In rare cases, Turner syndrome can be inherited if one parent carries a chromosomal abnormality.


Turners syndrome is what type of disorder?

Turner syndrome is a genetic disorder caused by a missing or incomplete X chromosome in females. It is characterized by specific physical features and can lead to health issues such as short stature and infertility.


What can be diagnosed by examining a karyotype of an individuals white blood cells?

A karyotype of an individual's white blood cells can be used to diagnose chromosomal abnormalities such as Down syndrome, Turner syndrome, and Klinefelter syndrome. It can also detect genetic disorders caused by aneuploidy or large structural chromosomal changes.


Does turner syndrome affect a certain demographic?

No, as it is a chromosomal disorder I am fairly sure it would affect all demographics equally.