How Do You Spell CHROMOSOMAL TRANSLOCATION?

Pronunciation: [kɹˈə͡ʊməsˌɒmə͡l tɹanslə͡ʊkˈe͡ɪʃən] (IPA)

The spelling of the word "Chromosomal Translocation" can be explained using IPA phonetic transcription. The word is pronounced as /ˌkrəʊməˈsəʊməl trænsloʊˈkeɪʃən/. The phonetic symbols show that the word begins with an unstressed syllable, "kro", followed by a stressed syllable, "mo", and ends with a stressed syllable, "shun". The vowels in each syllable are pronounced clearly, with the letter "o" pronounced as /əʊ/ in the first and second syllables, and as /oʊ/ in the third syllable. The consonants are pronounced similarly to the spelling of the word.

CHROMOSOMAL TRANSLOCATION Meaning and Definition

1. Chromosomal translocation refers to a type of genetic mutation that involves an abnormal rearrangement of genetic material between non-homologous chromosomes. It occurs when a segment of one chromosome is mistakenly transferred to another chromosome, resulting in the exchange of genetic material.

   During chromosomal translocation, two chromosomes break at their respective sites, and the broken ends fuse with each other. As a result, the chromosomes involved may have a piece that is out of its original position, leading to a rearrangement of genetic material. This process can occur in any type of chromosome, including autosomes (non-sex chromosomes) and sex chromosomes.

   Chromosomal translocations can have significant implications for an individual's health and development. Depending on the specific chromosomes involved and the location of the translocation breakpoints, it can disrupt the proper functioning of genes or alter gene expression patterns. This disruption can lead to a wide range of genetic disorders, including cancer, birth defects, and infertility.

   There are two main types of chromosomal translocations: reciprocal translocation and Robertsonian translocation. Reciprocal translocation occurs when two non-homologous chromosomes exchange segments, while Robertsonian translocation involves the fusion of two acrocentric chromosomes (chromosomes with centromeres located close to one end).

   Chromosomal translocation can be detected through genetic testing methods such as karyotyping or fluorescence in situ hybridization (FISH). These techniques enable the visualization and identification of chromosomal abnormalities, assisting in the diagnosis and management of related genetic disorders.

Common Misspellings for CHROMOSOMAL TRANSLOCATION

• xhromosomal translocation
• vhromosomal translocation
• fhromosomal translocation
• dhromosomal translocation
• cgromosomal translocation
• cbromosomal translocation
• cnromosomal translocation
• cjromosomal translocation
• curomosomal translocation
• cyromosomal translocation
• cheomosomal translocation
• chdomosomal translocation
• chfomosomal translocation
• chtomosomal translocation
• ch5omosomal translocation
• ch4omosomal translocation
• chrimosomal translocation
• chrkmosomal translocation
• chrlmosomal translocation
• chrpmosomal translocation

Etymology of CHROMOSOMAL TRANSLOCATION

The word "chromosomal translocation" is comprised of two components: "chromosomal" and "translocation".

"Chromosomal" refers to the chromosomes, which are long thread-like structures made up of DNA and proteins found in the nucleus of cells. They carry the genetic information necessary for the development, functioning, and reproduction of living organisms.

"Translocation" is derived from the Latin word "translocare", meaning "to transfer" or "to transport". In the context of chromosomal translocation, it signifies the process of the movement or transfer of a portion of one chromosome to another chromosome.

When these two components are combined, "chromosomal translocation" refers to a genetic alteration or rearrangement, where a segment of one chromosome breaks off and attaches to a different chromosome.

Plural form of CHROMOSOMAL TRANSLOCATION is CHROMOSOMAL TRANSLOCATIONS