1. The primary intended audience is couples ages 30-45 seeking genetic counseling for prenatal services. 2. The likely secondary audiences are genetic counselors, possibly younger or older couples outside of the specified age range, and doctors used for referrals. 3. The purpose of the document is to explain the benefits of prenatal genetic counselling, procedures and tests used to find genetic abnormalities, and what to do with the information received through genetic counseling. 4. The goal of the document is to persuade couples who are interested in prenatal genetic counseling to take the next step, and make an appointment with a certified genetic counselor. 5. The primary audience must know what genetic counseling is, why getting tested
A couple that met at a Cystic Fibrosis Society support group is contemplating having children. They both had brothers who developed cystic fibrosis and they are concerned about the likelihood of having sons who have the disease. As a counselor, you are to answer the following two genetic counseling consult questions in addition to the five critical thinking questions that are listed below.
This case study talks about a couple, Mark and Cory who are dwarfs. They are afraid of becoming parents to a child who is different from them. They feel like if their child is not born like them they wont be capable of taking care of that child. Since they are little people they have made many arrangements in there living environment that suites their lifestyle. They also mention that being little is part of their culture now and that their lives should be seen as dignified as the lives of others. Mark and Cory decided to talk to a genetic counselor about the likelihood of PGD and how this might give them the opportunity of having a child just like them. However when they meet with the genetic counselor he ask the couple to consider
JL’s parents are wishing to have another child. Could they benefit from genetic testing and genetic counselling? Explain your answer.
I support the guidelines outlined by Kitcher for the use of genetic information because of their responsible and ethical nature. I believe that future generations will benefit as a direct consequence of these guidelines. I shall begin by defining eugenics as the study of human genetics to improve inherited characteristics of the human race by the means of controlled selective breeding.
Modern technologies are constantly advancing in a multitude of ways to the degree that scientists have gained enough knowledgeable about the human genome to be able to find specific genes during the embryonic stage of reproduction. Scientists have already begun to use this knowledge to allow parents the ability to select the sex of their child and screen for genetic diseases via preimplantation genetic diagnosis (PGD) with in vitro fertilization (IVF). Sex-selection has already created world-wide discussion regarding the ethics of such a situation. However, scientists are now looking toward germline engineering which will essentially allow parents to select and alter genetic traits of their children before implantation of the embryo into
The genetic counselor should have a great deal of experience in dealing with specific genetic diseases, including Tay Sachs disease. They would be able to provide a list of support groups and or families they could refer the Trosack 's to in order for them to relate to others who have been through the process before. This type of assistance is chosen as part of the interdisciplinary team to assist this couple, especially Rita in understanding what they will be going through and what emotions to expect in the process. It will
Picture a young couple in a waiting room looking through a catalogue together. This catalogue is a little different from what you might expect. In this catalogue, specific traits for babies are being sold to couples to help them create the "perfect baby." This may seem like a bizarre scenario, but it may not be too far off in the future. Designing babies using genetic enhancement is an issue that is gaining more and more attention in the news. This controversial issue, once thought to be only possible in the realm of science-fiction, is causing people to discuss the moral issues surrounding genetic enhancement and germ line engineering. Though genetic research can prove beneficial to learning how to prevent hereditary
The prenatal period is when quick changes in the fetal organs are vulnerable to organizing change and stability but also building internal working system to trigger emotional responses (McEwen et al. 2013). It is a critical time for brain development and the PFC (McEwen et al. 2013). It exposes a selection of long -term modifications on brain development and behaviour (Entringer et al. 2009). Prenatal exposure to stress affects hormones in the body including the physiology and anatomy that relate to increasing drug levels, cortical communication and more (Entringer et al. 2009). Fetal stress is any event that interrupts a fetal process in stability in the body. (Entringer et al. 2009). During pregnancy, maternal stress impends the fetal nervous system and shortens the length of maturation due to many issues and concerns affecting the mother (Entringer et al. 2009). During pregnancy, maternal psychosocial stress threatens the fetal nervous system and contracts the length of gestation (Entringer et al. 2009). High levels of placental corticotrophin- releasing hormone
Modern medicine now relies more and more on genetic science, so the demand for health care professionals who can assess and communicate these health issues is significantly increasing. This is because public awareness is growing in conjunction with scientific advances in reproductive technologies. Health care consumers now want genetics specialists who can provide highly accurate and advanced consultations regarding their unique genetic conditions. Most genetic counselors work with couples or single mothers who
Many medical advances are being made today in the area of genetics. One of the most talked about is prenatal genetic testing. The purpose of prenatal genetic testing is to obtain information on a baby's health before they are born. This new technology will definitely improve the quality of human life. Diseases will be diminished and through new advances some diseases might even be eliminated. Children will be at less risk to have major health problems in their lives adding positively to their life experience. Prenatal genetic testing will also affects society as a whole.
Transition: So what should we say about the positives and negatives of Pre-Implantation Genetic Diagnosis?
Analyze the benefits and limitations of genetic and reproductive sciences for individuals, families, and society.
2. Is it right to use genetic screening as a tool to keep tabs on their prospective enrollees?
Here is a real life story of a woman who has been greatly affected by genetic testing and has seen both the good and the bad of genetic testing. This is a story that was posted in an article called “6 Moms Share Their Real Prenatal Testing Stories” on the website “What to Expect” from Courtney from Lake Stevens, Washington about how genetic testing has affected her life. So for Courtney, a few weeks after her 13 week ultrasound and her quad screen her doctors told her she had a positive screen for Down syndrome. So at 17 weeks she had to go back in for another ultrasound and genetic counseling which according to kids health.org is counseling that allows a genetic counselor to evaluate the results of a genetic test with the parents and helps the parents understand and reach decisions on what to do next. Her ultrasound looked great but still had a positive screen for Down syndrome. So she was was recommended for either an amnio or verifi test. Courtney then went to genetic counseling and choose to have the verifi test done over the amnio. A week later her results came back negative for Down syndrome and confirmed the baby was a girl. Courtney said “I am glad we opted to get the verifi test done especially after the stress of getting a positive screening before. I like how that if the NIPT did turn out positive for Down syndrome, I could have prepared ahead of time for the care of a special needs child would require, rather than feeling completely caught off-guard at birth.”
In the United States, an estimated 2.3 million couples are considered infertile [Wekesser, 1996]. This creates a large need for infertility specialists and clinics specializing in fertility treatments. With the quickly advancing field of rep roductive services and the quest for creating better, healthier babies, a new service called Preimplantation Genetic Diagnosis (PGD) is being offered in conjunction with In vitro fertilization.