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Karyotypes and Aneuploidy Quiz

Total questions: 66

Worksheet time: 2hrs 12mins

Name
Class
Date
1.

What is a karyotype?

a)

A type of plant species

b)

A type of protein found in cells

c)

A type of weather pattern

d)

A visual appearance of the chromosomes in the cell nuclei of an organism

2.

What are chromosomal abnormalities and how do they occur?

a)

Changes in the number or structure of chromosomes due to errors in cell division, exposure to harmful substances, or genetic factors.

b)

Chromosomal abnormalities are caused by eating too much sugar

c)

Chromosomal abnormalities occur due to excessive exercise

d)

Chromosomal abnormalities are caused by exposure to sunlight

3.

What is trisomy and monosomy? Provide examples of each.

a)

Trisomy 8 and Monosomy 9

b)

Trisomy 18 (Edwards syndrome) and Monosomy 13 (Patau syndrome)

c)

Trisomy 16 and Monosomy 22

d)

Trisomy 21 (Down syndrome) and Monosomy X (Turner syndrome)

4.

Explain Klinefelter syndrome and its genetic cause.

a)

Klinefelter syndrome is caused by having an extra Y chromosome in males.

b)

Klinefelter syndrome is caused by a missing X chromosome in males.

c)

Klinefelter syndrome is caused by the absence of the Y chromosome in males.

d)

Klinefelter syndrome is caused by the presence of an extra X chromosome in males.

5.

Describe Turner syndrome ____.

a)

Turner syndrome is a genetic condition that affects females, where one of the X chromosomes is missing or partially missing.

b)

Turner syndrome is a condition that affects males, causing them to be taller than average and have increased fertility.

c)

Turner syndrome is a condition that has no physical effects on individuals, only affecting their mental health.

d)

Turner syndrome is a condition that causes individuals to be male or female with an extra X chromosome,

6.

What are the characteristics of Down syndrome?

a)

Intellectual disability, distinctive facial features, and certain health problems

b)

No intellectual disability, no distinctive facial features, and no health problems

c)

Low intelligence, normal facial features, and no health problems

d)

High intelligence, average facial features, and no health problems

7.

How is karyotyping used in diagnosing chromosomal abnormalities?

a)

It is used to count the number of genes in a chromosome

b)

It is used to measure the length of the chromosomes

c)

It helps to identify any missing, extra, or abnormal chromosomes.

d)

It helps to determine the blood type of an individual

8.

Discuss the impact of aneuploidy on human health.

a)

Aneuploidy is beneficial for human health

b)

Aneuploidy can lead to genetic disorders and developmental abnormalities, impacting human health.

c)

Aneuploidy has no impact on human health

d)

Aneuploidy only affects physical appearance, not health

9.

The difference between autosomal and sex chromosome aneuploidy:

a)

Autosomal aneuploidy involves an abnormal number of chromosomes in the non-sex chromosomes, while sex chromosome aneuploidy involves an abnormal number of chromosomes in the sex chromosomes.

b)

Autosomal aneuploidy involves an abnormal number of chromosomes in the sex chromosomes, while sex chromosome aneuploidy involves an abnormal number of chromosomes in the non-sex chromosomes.

c)

Autosomal aneuploidy and sex chromosome aneuploidy are the same and have no difference.

d)

Autosomal aneuploidy only affects females, while sex chromosome aneuploidy only affects males.

10.

What are the ethical considerations surrounding prenatal testing for aneuploidy?

a)

Increased risk of miscarriage

b)

Limited access to prenatal testing

c)

Financial burden on the healthcare system

d)

Ethical considerations include potential discrimination, emotional impact, and selective termination.

11.

Which Genetic syndrome can we observe in this karyotype?

a)

Turner

b)

Klinefelter's

c)

Down

d)

Edward's

12.

Which Genetic syndrome can we observe in this karyotype?

a)

Turner

b)

Edward's

c)

Pateau

d)

Klinefelter's

13.

What is the gender of this person?

a)

Male

b)

Female

14.

What syndrome does this person have and what is their gender?

a)

Male

b)

Female

c)

Edwards

d)

pateau

e)

down

15.

Pairs of similar chromosomes are called...

a)

homologous chromosomes

b)

sister chromatids

16.

What is an organized picture of all of an organism’s homologous chromosome pairs lined up with each other?

a)

Pedigree

b)

Karyotype

17.

Which of the following is used to determine genetic defects or if an extra or missing chromosome exist in an organism?

a)

Pedigree

b)

Punnett Square

c)

Karyotype

18.

Which type of chromosome determines if someone will be male or female?

a)

autosomes

b)

sex chromosomes

19.

Which set of chromosomes represents a male?

a)

XX

b)

XY

20.

Which set of chromosomes represents a female?

a)

XX

b)

XY

21.

Cells that contain 2 sets of chromosomes are called ...

a)

haploid

b)

diploid

22.

How many pairs of autosomes do human cells contain?

a)

22

b)

1

c)

46

23.

How many pairs of sex chromosomes do human cells contain?

a)

22

b)

1

c)

46

24.

How many total chromosomes do human cells contain?

a)

23

b)

46

25.

What is a?

a)

Replicated chromosome

b)

sister chromatids

c)

Homologous chromosomes

26.

What is c?

a)

Replicated chromosome

b)

sister chromatids

c)

Homologous chromosomes

27.

What is d?

a)

Replicated chromosome

b)

sister chromatids

c)

Homologous chromosomes

28.

What is b?

a)

centriole

b)

centromere

29.

What is the mutation in this persons chromosomes?

a)

There is only one X

b)

7 is shaped like a hockey stick

c)

There's an extra 21

d)

1 is too curved

30.

This disorder is called "Cry of the cat", can you find the chromosomal mutation?

a)

There are too many chromosomes

b)

They are missing the Y chromosome

c)

Chromosome 1 is bent

d)

Chromosome 5 is too short (missing a piece)

31.

This person has Angel Mans syndrome. What is different about their chromosomes?

a)

Chromosome 1 is misshapen

b)

Chromosomes 21 is too small

c)

They are missing one of chromosome 15

d)

Chromosomes 7 and 8 look weird

32.

This is known as Edwards Syndrome, can you identify the chromosomal mutation?

a)

Chromosomes 1 and 2 are bent

b)

There is no Y chromosome

c)

This persons chromosomes are normal

d)

There are 3 of chromosomes 18

33.

Which phase of the cell cycle is when scientists take a picture to construct a karyotype?

a)

Interphase

b)

Prophase

c)

Metaphase

d)

Anaphase

34.

Homologous pairs:


(select all that apply)

a)

Have the same genes on them

b)

May have different alleles

c)

Each comes from one parent

d)

Combine to give you your genotypes

35.

Which of the following is a result of a nondisjunction?

a)

Klinefleter syndrome

b)

Sickle cell anemia

c)

Cystic fibrosis

d)

Hemophilia

36.
Which disease or disorder is the result of having an extra chromosome?
a)
Cystic Fibrosis
b)
Down Syndrome
c)
Colorblindness
d)
Sickle-cell Disease
37.

44 + X

a)

Klinfelter's syndrome

b)

Cystic Fibrosis

c)

Down's Syndrome

d)

Turner's Syndrome

38.

44 + XXY

a)

Klinfelter's syndrome

b)

Cystic Fibrosis

c)

Down's Syndrome

d)

Turner's Syndrome

39.

In which phase does crossing-over happen?

a)

Prophase I

b)

Prophase II

c)

Metaphase I

d)

Anaphase II

40.

During meiosis, if an organism has 10 chromosomes, how many will the new daughter cells have?

a)

10

b)

8

c)

5

d)

2

41.
How many chromosomes do humans have?
a)
46-- 23 from mom, 23 from dad
b)
22--11 from mom, 11 from dad
c)
10-- 5 from mom, 5 from dad
d)
23
42.

This term refers to half the normal chromosome number

a)

haploid

b)

2N

c)

diploid

d)

3N

43.

The exchange of genetic information that insures that every gamete is unique is referred to as

a)

mitosis

b)

meiosis

c)

reduction division

d)

crossing over

44.

All sperm and egg cells are genetically identical.

a)

TRUE

b)

FALSE

45.

The term that refers to a cell that has its full or complete number of chromosomes is

a)

diploid

b)

N

c)

gamete

d)

haplpoid

46.

At the end of meiosis, how many complete/operational sex cells are created for each original cell?

a)

2 for males; 2 for females

b)

1 for males; 4 for females

c)

4 for males; one for females

d)

1 for males; 1 for females

47.

Sea turtles have 56 chromosome in their somatic cells. How many chromosomes are in their gametes?

a)

28

b)

56

c)

112

d)

46

48.
During which stage of interphase does the cell replicate its DNA?
a)
G!
b)
S
c)
G2
d)
All 3 stages
49.

A pair of identical chromosomes (one inherited from mom and one inherited from dad) are called ______________________________.

a)

sister chromotids

b)

centromeres

c)

homologous chromosomes

d)

autosomes

50.

The failure of one or more pairs of homologous chromosomes or sister chromatids to separate "normally" during meiosis is called _____________________.

a)

nondisjunction

b)

anaphase I

c)

nondiploidy

d)

karyotype

51.

Nondisjunction

a)

When a segment of a chromosome breaks off.

b)

When a segment of a chromosome breaks off, flips, and reattaches.

c)

When a segment of a chromosome breaks and attaches to a non homologous chromosome.

d)

When entire chromosomes don't separate evenly during meiosis.

e)

When a segment of a chromosome is copied or doubles.

52.

This Karyotytpe belongs to which syndrome?

a)

Turner Syndrome

b)

Edwards Syndrome

c)

Patau Syndrome

d)

Down Syndrome

e)

Klinefelter Syndrome

53.

This karyotype belongs to which syndrome?

a)

Patau's Syndrome

b)

Edward's Syndrome

c)

Klinefelter Syndrome

d)

Down Syndrome

54.

Non-disjunction involving the X chromosomes occurs during oogenesis and produces two kinds of eggs, XX and O (no X chromosomes). If normal sperms fertilize the two types of eggs, which are the possible genotypes produced?

a)

XX AND XY

b)

XYY AND XO

c)

XXY AND XO

d)

YY AND XO

55.

In a _______________________ one chromosome of a homologous pair is missing. In a ______________________the affected person has three copies of one of the chromosomes instead of two. Down syndrome is an example of a _________________ while Turner syndrome is an example of a _____________________.

a)

monosomy, trisomy, trisomy, monosomy

b)

trisomy, monosomy, monosomy, trisomy

56.

The inheritance of an extra chromosome is called:

a)

monosomy

b)

trisomy 21

c)

aneuploidy

d)

trisomy

57.

A diploid cell that is missing one chromosome of a homologous pair is called a:

a)

aneuploidy

b)

monosomy

c)

nondisjunction

d)

trisomy

58.

The karyotype in the diagram is from an infant with a high-pitched cry that sounds like that of a cat. Which syndrome do they have?

a)

Klinefelter

b)

Down

c)

Cris-du-chat

d)

Turner

59.

Select an example of aneuploidy:

a)

Triploidy

b)

Tetraploidy

c)

Biploidy

d)

Trisomy

60.

Select an example of euploidy in humans:

a)

44 XXY

b)

44 XX

c)

3n

d)

44 X0

61.

Which of these is not an indication for karyotyping?

a)

Leukemia

b)

Recurrent miscarriages

c)

Cousin with chromosomal abnormality

d)

First baby

62.

The name given to cells: a) containing more than one pair of homologous chromosomes is ​ (a)   as we see in strawberries with 5n. b) containing one extra chromosome is known as a ​ (b)   , c) while containing one less chromosome is known as a (c)   .

Choose from the below words
polyploidy
trisomy
monosomy
euploidy
63.

Nondisjunction in meiosis 1 means

a)

50% of gametes will be normal, 50% will be trisomy

b)

50% of gametes will be normal, 50% will be monosomy

c)

50% of gametes will be missing a chromosome; 50% will have one extra chromosome

d)

50% of gametes will be normal, 25% will be one extra chromosome, 25% will be missing a chromosome

64.

Nondisjunction in meiosis 1 means

a)

all gametes are affected with aneuploidy

b)

half the gametes are affected with aneuploidy

c)

all gametes are polyploid

d)

all gametes are euploid (normal)

65.

Nondisjunction in meiosis 2 means

a)

all gametes are affected with aneuploidy

b)

half the gametes are affected with aneuploidy

c)

all gametes are polyploid

d)

all gametes are euploid (normal)

66.

Nondisjunction occurs in spermatogenesis meiosis 2. That means ___

a)

50% will have 'n' chromosomes, 50% may have one extra chromosome

b)

50% will have 'n' chromosomes, 50% may be missing a chromosome

c)

50% are missing one chromosome ; 50% have one extra chromosome

d)

50% of the gametes will be normal, 25% will have an extra chromosome is fertilized, 25% will be missing a chromosome