answersLogoWhite

0

The chromosomal alteration that has the most drastic consequence is deletion. It is defined as the loss or absence of a section from a nucleic acid molecule or chromosome and usually result in some type of syndrome.

User Avatar

Wiki User

10y ago

What else can I help you with?

Continue Learning about Natural Sciences

Why are chromosomal alterations called syndromes not diseases?

Chromosomal alterations are called syndromes because they are a collection of symptoms that tend to occur together and are associated with a specific chromosomal abnormality. This differs from diseases, which are characterized by specific pathological processes or biochemical changes in the body. Chromosomal syndromes are typically caused by genetic mutations that result in a distinct set of physical and developmental characteristics.


What is the most change in the sequence of bases in a DNA molecule is most accurately referred to?

A mutation is the most accurate term for a change in the sequence of bases in a DNA molecule. Mutations can be caused by various factors and can result in alterations in the genetic information carried by the DNA.


What is chromosomal reaction?

A chromosomal reaction refers to the changes or responses of chromosomes in response to various stimuli, such as environmental factors, DNA damage, or during cellular processes like division. These reactions can include alterations in chromosome structure, such as breaks or rearrangements, and can impact gene expression and cellular function. Chromosomal reactions are significant in fields like genetics and cancer research, as they can lead to mutations and contribute to diseases.


What factors most affect Chromosomal abnormalities?

Factors that most affect chromosomal abnormalities include advanced parental age, exposure to certain environmental toxins or radiation, and genetic predisposition. Additionally, errors during cell division or replication can also lead to chromosomal abnormalities.


What is the most common chromosomal abnormality in humans?

The most common chromosomal abnormality in humans is Down syndrome, which is caused by an extra copy of chromosome 21. It occurs in about 1 in 700 births.

Related Questions

Why are chromosomal alterations called syndromes not diseases?

Chromosomal alterations are called syndromes because they are a collection of symptoms that tend to occur together and are associated with a specific chromosomal abnormality. This differs from diseases, which are characterized by specific pathological processes or biochemical changes in the body. Chromosomal syndromes are typically caused by genetic mutations that result in a distinct set of physical and developmental characteristics.


How much does it cost to have a wedding dress altered 2 sizes?

The cost of alterations to a wedding dress depends on how drastic the alterations are, where the dress is purchased, how quickly the alterations must be finished, and if any materials are needed for the alterations. Most dress boutiques have an on-site alterations specialist or tailor who can discuss the alterations (and their cost) you are considering for your wedding dress.


Why are the consequences of chromosomal alterations referred to as syndromes and not diseases?

They are syndromes because they have variable phenotypes


What are the limitations of ultrasound in genetic testing?

This procedure, however, cannot detect biochemical or chromosomal alterations in the fetus.


Are asbestos considered a chemical mutagen responsible for chromosomal mutations?

Yes, asbestos is considered a chemical mutagen that can cause chromosomal mutations. Exposure to asbestos fibers can lead to DNA damage, chromosomal alterations, and mutations in cells, increasing the risk of developing cancer.


What is the most change in the sequence of bases in a DNA molecule is most accurately referred to?

A mutation is the most accurate term for a change in the sequence of bases in a DNA molecule. Mutations can be caused by various factors and can result in alterations in the genetic information carried by the DNA.


Which types of mutation affects more genes a gene mutation or a chromosomal?

a gene is passed on from generations and a chromosome is just found in certain cells


Which of the following could be described as a chromosomal mutation?

A deletion, inversion, or translocation of a chromosome would be considered chromosomal mutations. These alterations involve changes in the structure or number of chromosomes, leading to genetic variations and potential health consequences.


What is chromosomal reaction?

A chromosomal reaction refers to the changes or responses of chromosomes in response to various stimuli, such as environmental factors, DNA damage, or during cellular processes like division. These reactions can include alterations in chromosome structure, such as breaks or rearrangements, and can impact gene expression and cellular function. Chromosomal reactions are significant in fields like genetics and cancer research, as they can lead to mutations and contribute to diseases.


What is a sudden change in chromosomes called?

A sudden change in chromosomes is called a chromosomal mutation. This can involve alterations in the structure or number of chromosomes. Examples include deletions, duplications, inversions, or translocations.


The genetic code is carried by the molecule in most organisms. chromosomal DNA guanine hereditary?

The genetic code is carried by the molecule in most organisms. chromosomal DNA guanine hereditary?


What factors most affect Chromosomal abnormalities?

Factors that most affect chromosomal abnormalities include advanced parental age, exposure to certain environmental toxins or radiation, and genetic predisposition. Additionally, errors during cell division or replication can also lead to chromosomal abnormalities.