Why Do People With Down Syndrome Have 47 Chromosomes?
Down syndrome occurs due to an extra chromosome 21, resulting in a natural genetic condition with 47 chromosomes.
When we look at the developmental process, the origin of this condition is based on the moment of fertilization. As reproductive cells from the mother and father combine, chromosomes are supposed to separate evenly. However, sometimes a situation called nondisjunction occurs, meaning the chromosomes fail to separate properly. In this case, the 21st chromosome does not divide and remains as an extra copy in a single cell. As a result, the embryo develops with three copies of chromosome 21. This genetic structure is transferred to all cells in the body. The extra chromosome affects many areas, from brain development and the immune system to muscle structure and learning processes. However, this effect does not appear the same in every individual. Each person’s genetic structure and environmental conditions are different, so the characteristics of people with Down syndrome can vary widely. The important point is that this is not a defect, but a natural genetic difference. Individuals with Down syndrome can adapt to society, receive education, work, and develop independent living skills.
The reason people with Down syndrome have 47 chromosomes is the presence of an extra copy of chromosome 21. This is a completely biological and genetic process; it does not develop later in life and is not caused by environmental factors. The cause is congenital and purely genetic. Therefore, Down syndrome should not be viewed as a disease, but as a genetic variation. As accurate information in society increases, prejudices decrease and the quality of life of individuals with Down syndrome improves. Knowledge, awareness, and understanding are the strongest tools in this process, because real change begins with knowing and understanding people. /