Deletion

Deletion is a term used in genetics to describe a mutation where a part of a chromosome or a sequence of DNA is lost during DNA replication. This can cause serious genetic disorders when the deletion includes genes or important regulatory regions.

Causes[edit | edit source]

Deletions can be caused by errors in DNA replication, meiosis, or mitosis. They can also be induced by environmental factors such as exposure to certain chemicals or radiation.

Types of Deletions[edit | edit source]

There are two main types of deletions: interstitial and terminal.

Interstitial Deletions: An interstitial deletion occurs when a segment of a chromosome is lost from the middle. This type of deletion can lead to a variety of genetic disorders depending on the genes that are lost.

Terminal Deletions: A terminal deletion occurs when a segment of a chromosome is lost from the end. This type of deletion can also lead to various genetic disorders.

Effects[edit | edit source]

The effects of deletions can vary greatly depending on the size of the deletion and the location in the genome. Small deletions may have little to no effect, while larger deletions can cause serious genetic disorders. Some of the disorders caused by deletions include Cri du chat syndrome, Williams syndrome, and Prader-Willi syndrome.

Detection[edit | edit source]

Deletions can be detected using various techniques such as karyotyping, fluorescence in situ hybridization (FISH), and comparative genomic hybridization (CGH).

Treatment[edit | edit source]

There is currently no cure for genetic disorders caused by deletions. Treatment typically focuses on managing symptoms and improving quality of life.

References[edit | edit source]

Deletion Resources
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