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Chromosomal Abnormalities

Chromosomal Abnormalities

Assessment

Presentation

Biology

12th Grade

Hard

NGSS
HS-LS3-1, HS-LS3-2, HS-LS1-3

+1

Standards-aligned

Created by

Ashley Chassard

FREE Resource

17 Slides • 19 Questions

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Multiple Choice

Which of the following is NOT a type of chromosomal abnormality caused by breakage of chromosomes?

1

Deletion

2

Duplication

3

Nondisjunction

4

Translocation

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Multiple Choice

What is nondisjunction and how does it affect chromosome number in daughter cells during meiosis?

1

Nondisjunction is the failure of chromosomes to separate properly during mitosis, leading to identical daughter cells.

2

Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate during meiosis, resulting in daughter cells with too many or too few chromosomes.

3

Nondisjunction is the process by which chromosomes replicate twice during meiosis, causing extra chromosomes in daughter cells.

4

Nondisjunction is the separation of chromosomes during mitosis, resulting in cells with half the chromosome number.

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Multiple Choice

Compare the effects of nondisjunction in Meiosis I and Meiosis II on the chromosome number of resulting gametes.

1

Nondisjunction in Meiosis I results in all gametes having the correct chromosome number, while Meiosis II results in all gametes having incorrect numbers.

2

Nondisjunction in Meiosis I results in half of the gametes having incorrect chromosome numbers, while Meiosis II results in all gametes having incorrect numbers.

3

Nondisjunction in Meiosis I results in all gametes having incorrect chromosome numbers, while nondisjunction in Meiosis II results in half of the gametes having incorrect numbers.

4

Both Meiosis I and Meiosis II nondisjunction result in the same number of incorrect gametes.

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Open Ended

Explain the difference between trisomy and monosomy and how each condition arises from nondisjunction.

10

Hotspot

Select the abnormal set of chromosomes in the picture provided.

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Multiple Select

Human chromosome disorders often result from biochemical imbalance. List two possible regulatory molecules that may be affected and describe their role in development.

1

hormones

2

transcritpion factors

3

low cAMP

4

improper ligand binding

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Fill in the Blanks

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Multiple Choice

Which of the following statements about the relationship between maternal age and the incidence of Down syndrome is correct?

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The incidence of Down syndrome decreases as maternal age increases.

2

The incidence of Down syndrome remains constant regardless of maternal age.

3

The incidence of Down syndrome increases as maternal age increases.

4

Maternal age has no effect on the incidence of Down syndrome.

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Multiple Choice

Which genetic testing procedure is used in the 2nd trimester to analyze the karyotype of an embryo?

1

Amniocentesis

2

Ultrasound

3

Blood test

4

MRI

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Open Ended

Explain how abnormalities in sex chromosomes can lead to distinct syndromes in humans. Use examples from the slides.

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Multiple Select

Which of the following are characteristics of Klinefelter’s syndrome (XXY male)?

1

Sterile

2

Tall

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Normal intelligence

4

Delayed emotional maturity

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Fill in the Blanks

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Open Ended

Compare the karyotypes shown for Klinefelter’s syndrome and Jacob’s syndrome. What is the key chromosomal difference between these two conditions?

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Multiple Choice

What is the biological reason that females with Trisomy X (XXX) are generally healthy?

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All but one X chromosome is inactivated

2

The extra X chromosome is deleted

3

The extra X chromosome is duplicated

4

The extra X chromosome is converted to a Y chromosome

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Fill in the Blanks

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Multiple Choice

Which of the following is NOT a typical symptom or characteristic of Turner syndrome?

1

Webbed neck

2

Short stature

3

Sterile

4

Excessive height

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Open Ended

Explain how changes in chromosome structure such as deletion, duplication, inversion, and translocation can impact genetic disorders. Use examples from the images.

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Multiple Choice

Which of the following is NOT a type of chromosomal breakage abnormality?

1

Deletion

2

Duplication

3

Nondisjunction

4

Inversion

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Open Ended

What are some possible consequences of errors during meiosis, and how might they affect an individual?

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