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2025 National Preliminary biology Topic 50 Free

Chromosomal abnormalities and disorders

Down syndrome (trisomy 21) from chromosomal nondisjunction · Sub-topic 1

PRELIMINARY STAGE 2025

Nglesie Amanfro SHS: 21 points

St Thomas Aquinas: 62 points

Bawku SHS: 40 points

QUESTION

Name the genetic condition caused by an unusual cell division which results in an extra or partial copy of chromosome 21.

ANSWER: Down syndrome

EXPLANATION

Down syndrome (trisomy 21) most commonly results from nondisjunction during meiosis, where chromosome 21 fails to separate properly, leaving a gamete (and resulting embryo) with three copies of chromosome 21 instead of the usual two.

PRACTICE QUESTIONS

1. How many chromosomes does a person with Down syndrome have?

ANSWER: Forty-seven.

2. What is nondisjunction?

ANSWER: The failure of chromosomes to separate properly during cell division.

3. What is a karyotype?

ANSWER: A picture of the chromosomes of a cell arranged in pairs.

4. Which maternal factor increases the risk of Down syndrome?

ANSWER: Older age of the mother.

5. State two features of Down syndrome.

ANSWER: Learning difficulty and a characteristic facial appearance.

6. Which test can detect Down syndrome before birth?

ANSWER: Amniocentesis.

7. What is translocation Down syndrome?

ANSWER: A form in which part of chromosome 21 is attached to another chromosome.

8. Name two other trisomies.

ANSWER: Edwards syndrome (18) and Patau syndrome (13).

9. What is Turner syndrome?

ANSWER: A condition in which a female has only one X chromosome.

10. What is Klinefelter syndrome?

ANSWER: A condition in which a male has XXY chromosomes.

11. What are autosomes?

ANSWER: Chromosomes that are not sex chromosomes.

12. In which division does nondisjunction occur?

ANSWER: In meiosis (or mitosis).