Preview

Genetic Counselor Decision Making

Good Essays
Open Document
Open Document
552 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Genetic Counselor Decision Making
Genetic Counselor Decision-Making

Two parents, Jenny and Bob Miller, are both well educated and rich. They have two children, James and Andrew, who are both stricken with muscular dystrophy. The prognosis is that their muscular systems will gradually deteriorate, resulting in an early death. Yet the advances of medicine hold out the promise of a possible cure in the foreseeable future with gene therapy. Closer to hand is the possibility that embryonic muscle cells from normal individuals might be injected into people suffering from muscular dystrophy, which could bring about partial relief for James and Andrew. There are risks, however, as with any experimental method, such as the possibility of immunological rejection of the foreign cells.

As their genetic counselor, what recommendations do you have for Jenny and Bob Miller?

Potential Items to research:

Muscular Function
Muscular Dystrophy
Scientific Research and Politics
Role of FDA
Family Health Care Decisions

Summarize your suggestions in a full page, 12-point font, double-spaced. Justify your decision.

Source: Modified from: HYPERLINK "http://ublib.buffalo.edu/libraries/projects/cases/davis_notes.html" http://ublib.buffalo.edu/libraries/projects/cases/davis_notes.html

SUGGESTIONS!

Hello. I am your genetic councilor. How are you? Your situation is pretty hard, I know. It must be hard going through all this trouble. You must be getting panic attacks, every now and then. I know, it is hard. Well, you know this is the 21st century there is GOT to be a way out all this trouble!. You've probably heard from the doctors that there is this treatment for muscular dystrophy, but, of course, there are risks. My recommendation? I think you should take the risks...

As you may know, Muscular Dystrophy is a disorder that weakens a person's muscle. More than 50,000 people are diagnosed with that kind of disorder. They usually come from the

You May Also Find These Documents Helpful

  • Good Essays

    case study

    • 1194 Words
    • 4 Pages

    1. Dunchenne muscular dystrophy is a genetic disorder due to progressive weakness and degeneration of muscle cells over time, discovered by Guillaume Duchenne.…

    • 1194 Words
    • 4 Pages
    Good Essays
  • Powerful Essays

    Anatomy Case paper

    • 2241 Words
    • 9 Pages

    Muscular Dystrophy: is a group of inherited disorders that involve muscle weakness and muscle loss gradually decline over a period of time.…

    • 2241 Words
    • 9 Pages
    Powerful Essays
  • Good Essays

    Genetics Study Guide Ch 2-4

    • 12787 Words
    • 52 Pages

    Skin cells taken from patients were reprogrammed to give rise to almost any cell type (with a gene cocktail). Another cocktail stimulated their differentiation – sure enough the muscle cells were too big with rigid filaments and a different set of genes being expressed. Diseased cells then were tuned into a different set of signals than healthy cells.…

    • 12787 Words
    • 52 Pages
    Good Essays
  • Good Essays

    Muscular dystrophies are a group of genetic conditions characterized by progressive muscle weakness and wasting (atrophy). The Duchenne and Becker types of muscular dystrophy are two related conditions that primarily affect skeletal muscles, which are used for movement, and heart (cardiac) muscle. These forms of muscular dystrophy occur almost exclusively in males.…

    • 1511 Words
    • 6 Pages
    Good Essays
  • Good Essays

    What is Duchenne Muscular Dystrophy and where does it come from? Firstly, it is a kind of muscle dystrophy. The word dystrophy refers to when an organ or tissue wastes away. A muscle dystrophy is a group of many inherited disorders that cause loss of muscle tissue and weakness in muscles. Duchenne Muscular Dystrophy is a genetic disorder characterized by progressive muscle degeneration and weakness caused by a defective gene for dystrophin, a protein in the muscles, and founded by French neurologist Guillaume Benjamin Amand Duchenne in the late 19th century.…

    • 884 Words
    • 4 Pages
    Good Essays
  • Satisfactory Essays

    Spinal muscular atrophy [SMA] is a disorder in which, you have a loss of motor neurons. Your muscle symmetry is often off. In addition, there is muscle weakness in your spinal cord. This occurs in a hard time sitting up and holding your head up on your own. It is just like when you are a newborn and you need a pillow to sit on the couch. A few major causes of SMA are loss of motor neuron cells or nerve cell. This mutation leads to a deficiency of motor neuron cells or nerve cells. The disorder SMA is tied to the gene "SMN1" and tied to chromosome 5. A few symptoms of this disorder are- difficulty breathing lack of oxygen, difficulty eating, floppy posture, small amount of movement, and all these symptoms will gradually get worse over time. All these symptoms are at about a mild level in the beginning.…

    • 417 Words
    • 2 Pages
    Satisfactory Essays
  • Better Essays

    Duchenne muscular dystrophy also known as DMD is a rare genetic condition that could affects all race and cultures; mostly boys. Duchenne muscular dystrophy affects 1 in 500 boys in approximation. According to muscular dystrophy association 20,000 children are born with DMD worldwide and approximately, 35% are as a result of spontaneous genetic mutation (2014). The disease is an X-linked recessive inheritance that the mother passed it on. DMD has a progressive muscular degeneration and weakness and it is one of the nine types of muscular…

    • 1130 Words
    • 5 Pages
    Better Essays
  • Good Essays

    Unit 6 Assignment 1

    • 381 Words
    • 2 Pages

    Muscular Atrophy is a decrease in the mass of a muscle. This leads to muscle weakness. An 84-year old thin white female with this disease will be in constant discomfort and is already lacking in muscle because of her age and size and will become weak due to the decrease of muscle mass. She will be unable to perform certain tasks or worsen the risks of accidents while performing normal daily activities such as walking. This disease is common among the elderly. (Wikipedia, 2013)…

    • 381 Words
    • 2 Pages
    Good Essays
  • Good Essays

    In September of 1999, the Institute of Human Gene Therapy at the University of Pennsylvania ran an experiment in which Jesse Gelsinger participated (Rowe, 2000). The experiment consisted of an ornithine transcarbamylase gene therapy, wherein participants would increase their abilities to eliminate ammonia (Rowe, 2000). Because Gelsinger had a genetic disease (called ornithine transcarbamylase or OTC) which caused him to have difficulties in releasing ammonia from his body, he seemed to be an ideal participant (Kolehmainen, 2000). Unfortunately, neither Jesse nor his father were aware before the commencement of the experiment that several monkeys had died from the therapy, and human participants had been suffering adverse effects from the experiment (Rowe, 2000). Also, Jesse Gelsinger and the other participants involved were not…

    • 670 Words
    • 3 Pages
    Good Essays
  • Satisfactory Essays

    Duchenne muscular dystrophy is a genetically inherited disease that causes progressive muscle and bones weakness. The symptoms usually appear before age 6 and may appear as early as infancy. Symptoms can be noticed very early like not sitting and standing independently at the correct age. The age for walking for boys with Duchenne muscular dystrophy is around 18 months. There is progressive muscle weakness of the legs and pelvic muscles, which is caused by a loss of muscle mass. This muscle weakness can cause difficulty climbing stairs. Most Symptoms appear in boys ages 1-6. Because of muscle damage kids Might need braces by the age of 10 and by age of 12 be in be wheelchair. The amount of people using wheelchairs because of duchenne muscular dystrophy is around, 29% of males 5 through 9 years of age, 82% of males 10 through 14 years of age and more than 90% of males 15 through 24 years of age.…

    • 315 Words
    • 2 Pages
    Satisfactory Essays
  • Satisfactory Essays

    Mdx Mouse Model

    • 954 Words
    • 4 Pages

    Researchers across the globe have utilized various animal models to study DMD. The most common animal model used to study therapeutics for DMD is the mdx mouse owing to its low cost and easy accessibility. The mdx mouse, has a nonsense mutation in exon 23 of the Dmd gene that leads to complete loss of the dystrophin protein 12, 13. The mdx mouse model of DMD is not considered an ideal model for understanding the pathogenesis of DMD owing to significant differences in physiology from humans and display of milder phenotypes compared to DMD patients. The diaphragm muscle of the mdx mouse however, exhibits a pattern of degeneration, fibrosis and severe functional deficit comparable to that of human DMD limb muscle14 and is often the muscle…

    • 954 Words
    • 4 Pages
    Satisfactory Essays
  • Good Essays

    prenatal genetic testing

    • 495 Words
    • 2 Pages

    If the researchers can identify the sequences of genes they can correct the sequences related with disease and disability. Researchers had a less success using gene therapy to correct such conditions and no researchers had at least tried to use gene therapy to correct impairments in a fetus.…

    • 495 Words
    • 2 Pages
    Good Essays
  • Good Essays

    Genetic Counselor

    • 456 Words
    • 2 Pages

    Genetic Counselors are professional who have completed a master’s program in medical genetics and counseling skills. They then pass a certification exam administered by the American Board of Genetics Counseling. Genetic counselors can help and inheritance patterns, suggest testing, and lay out possible scenarios. They will explain the meaning of the medical science involved, provide support, confirming a diagnosis in a person who has disease symptoms, and address any emotional issues raised by the results of the genetic testing.…

    • 456 Words
    • 2 Pages
    Good Essays
  • Satisfactory Essays

    Those with muscular dystrophy are often hesitant when it comes to exercise. As anyone with the condition knows, exercise can take a toll but it can also do a lot of good. In fact, studies show that regular exercise can help make daily activities easier since it improves strength as well as flexibility and endurance. Those with muscular dystrophy can build nice, firm glutes just like everyone else. The only difference is the approach.…

    • 395 Words
    • 2 Pages
    Satisfactory Essays
  • Satisfactory Essays

    Lauren, I agree with you, genetic counseling is the family’s decision. As you stated, being the nurse, we must educate them and give them the most current information and literature so they can make an informed decision. We must support our clients in their decisions. As nurses, we must be culturally aware, we must put aside our cultural values since they may differ from their cultural values, which in turn allows the nurse to adjust their practices to do what is best for the family (Kaakinen, Coehlo, Steele, Tabacco, & Hansen, 2015).…

    • 92 Words
    • 1 Page
    Satisfactory Essays