Autosomal Dominant Genetic Disorders

Autosomal Dominant Genetic Disorders

Assessment

Interactive Video

Biology, Science, Other

9th - 12th Grade

Hard

Created by

Patricia Brown

FREE Resource

The video tutorial explains autosomal dominant inheritance using polycystic kidney disease as an example. It covers the expression of dominant and recessive genes, the formation of gametes, and the probability of inheriting the disease. The tutorial also generalizes these concepts to other autosomal dominant conditions like Huntington's chorea, emphasizing a 50% chance of inheritance for each child.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is an example of a disease caused by an autosomal dominant gene?

Sickle cell anemia

Polycystic kidney disease

Hemophilia

Cystic fibrosis

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In the context of genetic inheritance, what does it mean for a gene to be dominant?

It is expressed even if only one copy is present.

It is expressed only in males.

It is only expressed when two copies are present.

It is never expressed.

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the phenotypic result of having two recessive alleles for a trait?

No trait is expressed.

Both traits are expressed equally.

The recessive trait is expressed.

The dominant trait is expressed.

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

How does the presence of a dominant gene affect the expression of a recessive gene?

The recessive gene is always expressed.

The recessive gene is never expressed.

The recessive gene is expressed only if the dominant gene is absent.

The recessive gene is expressed only in females.

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the genotype of a person who is heterozygous for polycystic kidney disease?

Pp

pP

pp

PP

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the probability that a child will inherit polycystic kidney disease if one parent is heterozygous?

25%

100%

50%

75%

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the chance of a child being phenotypically normal if one parent is heterozygous for a dominant disease?

75%

50%

25%

0%

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