Final answer:
Tetrasomy is a chromosomal disorder characterized by having four copies of a particular chromosome. It is diagnosed through karyotype analysis and can cause various developmental and physical challenges due to the additional genetic material.
Step-by-step explanation:
What is Tetrasomy?
In the context of aneuploidies, tetrasomy is a chromosomal disorder where an individual has four copies of a particular chromosome instead of the normal two. This condition is a type of aneuploidy, which refers to an abnormal number of chromosomes in a cell. Unlike trisomy, where there are three copies of a chromosome, tetrasomy entails an additional pair, leading to the presence of extra genetic material. This excess can disrupt the delicate balance of gene expression and cause developmental and physical problems.
To diagnose such chromosomal anomalies, a karyotype analysis is performed. This test involves taking a photograph of an individual's chromosomes, typically during metaphase of cell division, and arranging them in a standard format to identify any extra or missing chromosomes. For instance, trisomy 21 is visible on a karyotype as an extra chromosome 21, which is the cause of Down Syndrome—a well-known result of an aneuploidy.
Aneuploid conditions like tetrasomy and trisomy can occur due to nondisjunction during meiosis, where chromosomes fail to separate properly. In the case of tetrasomy, it means that a gamete was formed with an extra pair of a particular chromosome, which then gets replicated in all cells after fertilization, leading to an individual having four copies of that chromosome.