ANSWER
Classify the genetic disorders as single gene or chromosomal disorders.
Single gene disorder | Chromosomal disorder. |
* Huntington disease.(HTT gene mutation) * Duchenne muscular dystrophy.(DMD gene mutation) * Cystic fibrosis.(CFTR gene mutation) |
* Down syndrome.(Disorder of chromosome 21) * Klinefelter syndrome.(Presence of extra X chromosome XXY) |
classify the genetic disorder as single-gene or Chromosomal Huntington Disease Duchenne Muscular Distrophy Down Syn...
Is there an association between Duchenne muscular dystrophy (a rare disorder) and genetic risk? Select the MOST APPROPRIATE study design to answer his question: a. Cohort study b. Cross-sectional study c. Case-control study d. RCT
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...
Map a nursing care plan/clinical pathway for a patient with a specific genetic disorder (e.g., sickle cell disease, hemophilia, cystic fibrosis, Huntington disease). Prepare to discuss your care plan and rationales following a minimum of three nursing diagnosis for the disease specified.
Which of the following is not a genetic disorder? O Sickle Cell Disease O Tays Sachs Disease O Cystic Fibrosis O Teratogens
Marfan syndrome, a human genetic disorder caused by a single gene, results in defective connective tissue. The symptoms of this disorder range from skeletal issues to problems with the nervous and cardiovascular systems. This is an example of Question 17 2.1 pts Marfan syndrome, a human genetic disorder caused by a single gene, results in defective connective tissue. The symptoms of this disorder range from skeletal issues to problems with the nervous and cardiovascular systems. This is an example of...
gron's Disease is inherited as a dominant gene. Show with a Punnett square the chances of escaping this disease if one parent has it. Miss X has a sister with cystic fibrosis, a recessive genetic disorder. Mr. Z also has a sister with cystic fibrosis. Neither Miss X nor Mr. Z has CF. They want to start a family. The have decided to adopt children because the risk of having a child with cystic fibrosis is 50%. Are they correct...
Cystic fibrosis is an autosomal recessive disease caused by a mutation in a single gene with two alleles. Suppose the frequency of cystic fibrosis in a population is 3%. Assuming the gene is in HW equilibrium, calculate the allele and genotype frequencies. If the population consists of 100 individuals, how many are carriers (but unaffected) for the cystic fibrosis allele?
Question 7 0/0.5 Which of the following genetic disorders involves entire chromosomes? Cystic Fibrosis Huntington's Disease Sickle Cell Disease Down Syndrome Phenylketonuria
Question 5 0/0.51 Which of the following genetic disorders involves a single gene? Klinefelter syndrome Williams Syndrome Galactosemia Cri-du-Chat Syndrome Turner Syndrome
9. Cystic fibrosis is a genetic disease caused by an autosomal recessive allele at a single locus. In a survey of 100,000 people in Pennsylvania, 7 people had the disease. Assuming the population is in Hardy-Weinberg equilibrium, find: a. P: é o ö 10. How many people of 100,000 surveyed would you expect to be carriers of the cystic fibrosis allele?