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What is a Chromosomal aberration? Describe different types of chromosomal aberrations.

Introduction

Chromosomal aberrations refer to changes in the normal structure or number of chromosomes. These changes can lead to genetic disorders, developmental abnormalities, or even cancer. Chromosomal aberrations may occur due to errors during cell division, exposure to radiation, or chemical mutagens.

Definition

A chromosomal aberration is any change in the number or structure of chromosomes that results in genetic imbalance or abnormalities in an organism.

Types of Chromosomal Aberrations

I. Structural Chromosomal Aberrations

These involve changes in the structure of a chromosome due to breakage and incorrect rejoining.

1. Deletion

A segment of the chromosome is lost or deleted. It can be terminal (end) or interstitial (middle).

Example: Cri-du-chat syndrome (deletion on chromosome 5)

2. Duplication

A portion of the chromosome is duplicated, resulting in extra genetic material.

Example: Charcot-Marie-Tooth disease (duplication on chromosome 17)

3. Inversion

A segment of a chromosome is reversed end to end. It may be:

4. Translocation

A segment from one chromosome is transferred to another. Types include:

Example: Some forms of Down syndrome (translocation type)

II. Numerical Chromosomal Aberrations (Aneuploidy)

These involve an abnormal number of chromosomes.

1. Monosomy

One chromosome from a pair is missing (2n – 1).

Example: Turner Syndrome (XO)

2. Trisomy

One extra chromosome is present (2n + 1).

Examples:

3. Polyploidy

Presence of more than two complete sets of chromosomes. Common in plants, rare in humans.

Causes of Chromosomal Aberrations

Detection Methods

Conclusion

Chromosomal aberrations can significantly impact health and development. Understanding these changes helps in diagnosing genetic diseases, guiding treatment, and offering genetic counseling. Advanced diagnostic tools have improved early detection and management of these conditions.

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