Cystic fibrosis is a recessive , autosomal disorder. It is inherited from parents to off springs. The individual with the disease produce thick and sticky mucus. Such a mucus can block the passages of lungs, pancreas etc. It is life threatening and people with the condition have shorter life span.In this case both the partners are carriers of the disease , which the two of them found out after completing the genetic testing required. Such parents can have a child with the condition (cystic fibrosis). Punnet square results show that the probability of the child being cystic fibrosis patient is 1/4.

As per the punnet square 1/4 chance of the child being CF . So the parents need to take the decision or chance because 3/4 chance that the child will not be CF.
Chances of a person developing breast cancer are high if a person has BRCA gene. Such people need to be more careful and have regular check ups of the breast. Both self and also mammogram need to be regularly done. You may also consider taking some supliments that may prevent cancer in general. There are also instances when, such people under go mastectomy to avoid cancer development.
Care to prevent breast cancer would be healthy habits. 1. Prevent/ limit alcohol and tobacco. 2.Be physically active.
3.Control weight. 4. Breast feed the baby 5. Limit dose and duration of any hormone therapy
You decide to have genetic testing completed on you and your partner prior to having children....
Part 1: Make a T-chart showing the positive and negative aspects of personal genetic testing. [4 pts] Part 2: Answer the following questions. You decide to have genetic testing completed on you and your partner prior to having children. You find out that you and your partner are both carriers of Cystic Fibrosis. Show your Punnett square below. (NOTE: CF is not a sex-linked trait) How could you use the information given to you by the geneticist to make an...
1) You have been hired as a genetic counselor. Your first patient is a young woman named Lei who comes to you because her brother has cystic fibrosis. (Learn more about this disease in the PowerPoint slides – find out how it is inherited, is it dominant or recessive?) Lei is healthy but would like to know the risk that she is a carrier for the disease. Both her parents are healthy as is her older sister. a. Fill in...
Perhaps you an /or your significant other is a carrier of a harmful recessive trait, such as cystic fibrosis. What would you do when considering having children? Would you hope for the best and ignore the situation or would you see a genetic counselor or what? 2. Choose a genetic disorder other than those discussed in the class notes and tell us about it. You should include effects, survival rates etc.
For each of these problems, be sure to justify your answer(s) by including an allele key, parental cross (genotypes), phenotypes, and the resulting Punnett square representing all possible mating of eggs and sperm. 1. Tom and his wife Julie are both carriers for cystic fibrosis, an autosomal recessive disease. What is the chance that their children will have cystic fibrosis and carriers? 2. In cattle, a dominant “Dexter” gene, combined with its recessive allele, results in abnormally short legs, while...
Part III: Dr. Hernandez sits down with Ann and her partner. The doctor is sorry to report that Ann has breast cancer; however, because it was caught early and responds to estrogen and progesterone, the prognosis is good. At this point it looks like the cancer is stage 1. However, as Ann is young, the doctor wants to perform a couple tests. The first test is a genetic sequencing test for BRCA1 and BRCA2, as well as testing for other...
general biology
Dar eu.pl I al 0.97pm Quiz Instructions After you have completed Lab 11, watch and take detailed notes on the NOVA video Cracking Your Gene You may find it helpful to preview the quiz questions before you watch the video. You may use up to 3 att Note: You are not required to use the Respondus Lockdown Browser for this video quiz. Question 1 The difference between genotyping and gene sequencing is that genotyping is able to identify...
Match the following terms with the appropriate description
below:
a. alleles b. autosomes c. dominant allele d. genotype e.
heterozygous f. homozygote g. phenotype h. recessive allele i. sex
chromosomes
1. ________________ genetic make-up
2. ________________ how genetic make-up is expressed
3. ________________ chromosomes that dictate most body
characteristics
4. ________________ alternative forms of the same gene
5. ___________an individual bearing two alleles that are the same
for a particular trait 6. ________________ an allele that is
expressed, whether in...
Quiz 8: Genetics and Heredity Add relevant, accurate information for extra credit. Follow directions. Return on 4/s I) A woman has a cop y of the gene for an autosomal dominant disorder. This means: a. b. c. d. She will be a carrier of the disorder but won't have it She will have the disorder She will not have the disorder Her partner will have the disorder 2) Create a Punnett Square out of the following information about Tay-Sachs Dis...
90170021 201901/P53 pd 8. (3) Lator you find out that you have access to a microarray for 10 gones that are associated with John's type of cancer. The microarray was done comparing normal tissue the microarray are shown below. One of the patients is John sequence of proteins. What are these mutations? How do the mutations change the 9. (2) If you were to suggest gene therapy to the family. how you describe what the main goal of this therapy...
For this discussion board assignment, you will create a discussion board thread about a genetic disease of your choice. Think of your discussion board post as an informative (but brief!) summary teaching your classmates about the genetic disease. To get started, open the attached document of the List of Genetic Diseases Actions : (-Cystic Fibrosis -Down’s Syndrome -Duchenne Muscular Dystrophy Edward Syndrome -Familial Alzheimer Disease Familial Breast Cancer -Fragile X Syndrome Galactosemia -Hemophilia -Huntington’s Disease Ichthyosis -Incontinentia pigmenti Kleinfelter’s Syndrome...