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Copy of Genetic Disorders (5/28/2026)

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Last updated about 2 hours ago
15 questions
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What you will learn

  • Common genetic disorders in humans and how they are caused
  • Chromosomal disorders and their modes of inheritance
  • How genetic disorders are diagnosed and treated
Before you move on the body of the activity, it will be helpful to do a video review of some prior content that relates to this topic.
Question 1
1.
According to the video, a _______ is a short section of DNA that encodes for a single trait.
Question 2
2.
According to the video, humans inherit _______ chromosomes from their mother and _______ chromsomes from their father.
Question 3
3.
According to the video, on a karyotype, all of the chromosomes are paired together in _______ pairs, which are chromosomes that have the same size, shape, and information.
Question 4
4.
According to the video, on a karyotype, the first twenty-two pairs of chromosomes are called _______.
Question 5
5.
According to the video, sex chromosomes are called _______.

Is being short-statured inherited?

It can be. Achondroplasia is the most common form of dwarfism in humans, which can also be observed in other animals such as horses. In humans, it is caused by a dominant mutation. The mutation can be passed from one generation to the next.

Genetic Disorders

Many genetic disorders are caused by mutations in one or a few genes. Other genetic disorders are caused by abnormal numbers of chromosomes.

Genetic Disorders Caused by Mutations

The Table below lists several genetic disorders caused by mutations in just one gene. Some of the disorders are caused by mutations in autosomal genes, others by mutations in X-linked genes. Which disorder would you expect to be more common in males than females?
Few genetic disorders are controlled by dominant alleles; meaning that most are recessive disorders. A mutant dominant allele is expressed in every individual who inherits even one copy of it. If it causes a serious disorder, affected people may die young and fail to reproduce. Therefore, the mutant dominant allele is likely to die out of the population.

A mutant recessive allele, such as the allele that causes sickle cell anemia (see the Figure below), is not expressed in people who inherit just one copy of it. These people are called carriers. They do not have the disorder themselves, but they carry the mutant allele and can pass it to their offspring. Thus, the allele is likely to pass on to the next generation rather than die out.

Chromosomal Disorders

Mistakes may occur during meiosis that result in nondisjunction. This is the failure of replicated chromosomes to separate during meiosis. Some of the resulting gametes will be missing a chromosome, while others will have an extra copy of the chromosome. If such gametes are fertilized and form zygotes, they usually do not survive. If they do survive, the individuals are likely to have serious genetic disorders. The Table below lists several genetic disorders that are caused by abnormal numbers of chromosomes. Most chromosomal disorders involve the X chromosome. Look back at the X and Y chromosomes and you will see why. The X and Y chromosomes are very different in size, so nondisjunction of the sex chromosomes occurs relatively often.
Question 6
6.

What genetic disorder does the above karyotype represent? _______
Tip: use the table, just above, to assist you.
Question 7
7.

Question 8
8.
A male Hemophilia A patient has a male parent and a female sibling who do not have the Hemophilia A. What condition does the female parent have? _______
Tip: use the first table and the follow two paragraphs to assist you.

Diagnosing Genetic Disorders

A genetic disorder that is caused by a mutation can be inherited. Therefore, people with a genetic disorder in their family may be concerned about having children with the disorder. Professionals known as genetic counselors can help them understand the risks of their children being affected. If they decide to have children, they may be advised to have prenatal (“before birth”) testing to see if the fetus has any genetic abnormalities. One method of prenatal testing is amniocentesis. In this procedure, a few fetal cells are extracted from the fluid surrounding the fetus, and the fetal chromosomes are examined.

Treating Genetic Disorders

The symptoms of genetic disorders can sometimes be treated, but cures for genetic disorders are still in the early stages of development. One potential cure that has already been used with some success is gene therapy. This involves inserting normal genes into cells with mutant genes.

If you could learn your risk of getting cancer or another genetic disease, would you? Though this is a personal decision, it is a possibility. A number of companies now make it easy to order medical genetic tests through the Web.

Summary

  • Many genetic disorders are caused by mutations in one or a few genes.
  • Other genetic disorders are caused by abnormal numbers of chromosomes.
Question 9
9.
_______ symdrome is a genetic disorder caused by an extra copy of the twenty-first chromosome.
Question 10
10.
In _______ the shape of the red blood cells is affected.
Question 11
11.
Genetic disorders that are caused by a mutant dominant allele are likely to _______ of the population, meaning that they are not likely to be passed on to future generations.
Question 12
12.
_______ are not likely to be aware that they have a defective copy of a chromosome because they do not have the disorder themselves.
Question 13
13.
_______ is a mistake in which chromosomes do not separate during meiosis. This leads to extra copies of chromosomes in some sex cells (gametes) and missing copies of chromosomes in other sex cells.
Question 14
14.
A _______ is used to extract fluid around the fetus to test the chromosomes for the presence of a genetic disorder.
Question 15
15.
Generally, only the _______ of genetic disorders can be treated, however, gene therapy is begininng to show some promise of providing cures in the future.
In the above karyotype, the sex chromosomes are not shown. What abnormal sex chromosome condition in the above karyotype would represent Klinefelter syndrome (select all that apply)?
Tip: use the table, just above, to assist you.