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Newborn genetic screening summary
Of newborns require initial assessment
Immediate newborn exam
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The purpose of newborn genetic screening is to screen newborns for potential health concerns. Newborn genetic screening started in 1965 with the testing of one disorder, phenylketonuria (WDHS). Since then, newborn genetic screening has evolved and over 4 million newborns are screened in the U.S. every year (CCHC Report). Currently, in the state of Wisconsin, there are 47 different disorders that are tested for (WDHS). The process of screening newborns is a relatively short procedure. Before a newborn leaves the hospital a nurse pricks its heel and takes a few drops of blood and deposits it on a special test paper. The paper is then sent to a lab where technicians look for disorders in their genes. Wisconsin law (statues chapter 253.13) “requires that all babies born in hospitals in Wisconsin have newborn screening before they leave the hospital.” The screening costs $69.50 but is covered by most health insurances, if it’s not covered it is encouraged that contact is made with the Newborn Screening Coordinator at the Wisconsin Division of Public Health. However, $69.50 may be the price to pay for the peace of mind knowing that your baby is healthy. Sickle cell anemia is present in one out of every two African Americans (google health). Sickle cell anemia is passed down through families and makes red blood cells form in a crescent shape. However, red blood cells are normally a disc shape. This is a very painful disorder that requires ongoing treatment and without treatment life expectancy of the patient is dramatically decreased. With newborn genetic screening it’s possible to catch this disorder early in life and ensure the proper treatments that could save the newborns life. Discovering a hereditary disorder like sickle cell... ... middle of paper ... ...enetics.utah.edu/content/health/ngs/> • "Children and Youth with Special Health Care Needs Program Newborn Screening." Wisconsin Department of Health Services. 07 10 2009. Web. 20 Feb 2010. . • "Sickle Cell Anemia ." Google Health. Google , Web. 20 Feb 2010. https://health.google.com/health/ref/Sickle+cell+anemia • "Newborn Genetic Screening Mandate." Citizens Council on Healthcare . Web. 20 Feb 2010. . • Brase, Twila. "NEWBORN GENETIC SCREENING." Citizens Council on Healthcare . Web. 21 Feb 2010. . • "Genetic Counseling." genomics.energy.gov. 29 11 2008. Web. 21 Feb 2010. .
Advantages of genetic testing may be helpful in determining whether or not you have a disease or are proba...
Many methods of screening have been implemented including neonatal sampling of hair and meconium, maternal urine screening, and maternal self-reports.(11) In considering wide-spread feasibility, self-report measures have been commonly used, some more known and validated methods include the 4 P’s plus and TWEAK. (4,5,13) In the clinic visit, the Obstetrician may also implement a brief motivational interview to assess the patients willingness to change. The Treatment and Intervention Protocol recommends the FRAMES Approach where the providers give feedback, responsibility, advice, menus of change options, empathy, and empowers t...
The child that I tested will be referred to as K.L. I tested her on April 14th 2016. K.L. is 2 years old, with her exact age being 2 years 9 months and 14 days. I called and asked her mother if she would mind dropping K.L. off with me for a few hours so I could perform the test, and then pick her back up after the test was complete. This test more accurate when the caregiver is not present. K.L. has a step sister and a baby brother on the way. She has always been in the daycare setting, because her grandmother is a provider. K.L. was delivered full term via planned cesarean section due to her mother’s small pelvis. There was no complications during this pregnancy. K.L. weighted 8 lbs. 4 oz. and was 20 ½ inches long at birth, now weighting in at ...
Teutch, S., & Tuckson, R. Department of Health & Human Services, (2008). U.S. system of oversight of genetic testing: A response to the charge of the secretary of health and human services. Retrieved from website: http://osp.od.nih.gov/sites/default/files/SACGHS_oversight_report.pdf
Sickle cell anemia is a disease that has to be inherited from both parents. Both parents have sickle cell trait, which means each parent has sickle hemoglobin and normal hemoglobin. So people with the sickle cell trait can pass the sickle cell gene to their children. Most families that come from Africa, South Central, and Central America are more common with sickle cell anemia. According to National Heart, Lung and Blood, it’s estimated that the sickle cell disease has affected 70,000-100,000 people mainly African Americans (National Institute of Health, 2012). Hispanic Americans also are common to having sickle cell anemia. According to National heart, Lung, and Blood Institute, statistics shows sickle cell anemia occurs in about 1 out of every 500 African American births and 1 out of 36,000 Hispanic American births (National Institute of Health, 2012). Signs of sickle cell anemia don’t show until after 4 months of age. Sickle cell anemia begins from ...
Sickle cell anemia is a hereditary disorder that mostly affects people of African ancestry, but also occurs in other ethnic groups, including people who are of Mediterranean and Middle Eastern descent. More than 70,000 Americans have sickle cell anemia. And about 2 million Americans - and one in 12 African Americans - have sickle cell trait (this means they carry one gene for the disease, but do not have the disease itself).
In conclusion, it can been seen that newborn examination play an important part is assessing the neonates well-being, and that midwives need to be equipped with the necessary skills to conduct such examinations and encouraged and involve the mothers or family members in the examinations as well as planning for the care of the newborns.
have higher rates of low birth weighted need special care right after birth for times as
Within the past thirty years, researchers have found strong evidence linking genes and disease. The development of predictive genetic tests followed shortly after the isolation of certain candidate genes. Although predictive genetic screening is only available for a handful of diseases, its effects and ramifications have become hotly debated issues in a wide range of areas, from government to religion. The debate began in the 1993 when researchers isolated the BRCA1 gene, which is associated with increased risk of developing breast and ovarian cancer. The discovery of this gene led to excitement and speculation of developing a predictive genetic test to identify those women at risk for these cancers. In this paper, I will first describe the biology of genetic testing, and then discuss the pros and cons of predictive genetic testing.
Prenatal genetic testing has become one of the largest and most influencial advances in clinical genetics today. "Of the over 4000 genetic traits which have been distinguished to date, more than 300 are identifiable via prenatal genetic testing" (Morris, 1993). Every year, thousands of couples are subjecting their lives to the results of prenatal tests. For some, the information may be a sigh of relief, for others a tear of terror. The psychological effects following a prenatal test can be devastating, leaving the woman with a decision which will affect the rest of her life.
The "Genetic Screening" Genetic Screening. NDSU,. Web. The Web. The Web.
Genetic testing is the process of sequencing six billion letters of a human genome to possibly discover genetic differences, such as how cells carry the same genome but at the same time look and function different. Genetic testing is also the process that can give foresight into pathological diseases such as different types of cancer.
Genetic testing, also known as screening, is a rapidly advancing new scientific field that can potentially revolutionize not only the world of medicine, but many aspects of our lives. Genetic screening is the sequencing of human DNA in order to discover genetic differences, anomalies, or mutations that may prove pathological. As genetic screening becomes more advanced and easily accessible, it presents society with difficult questions that must be asked about the boundaries of science and to what degree we are allowed to tamper with the human genome. To better understand the potential impact of genetic screening on our society, we must examine the potential benefits in comparison to the possible negative impact it may cause. With this knowledge in hand, we can examine what the future holds for this field of study and the best possible direction to take.
Parents now have the possibility of testing genes for mutations and genetic problems (BBC News).
Newborn screening is the practice in which the harmful or potentially fatal conditions that can affect the infant's health or survival are detected. This process can prevent death or health problems and protect the infant against certain diseases and medical conditions. Newborn screening started in 1960's when many states in U.S.A. established a newborn test program for phenylketonuria (PKU) by using the Guthrie method, a system for the collection and transportation of blood samples on filter paper. Many Infants showed developments while receiving treatment. This success led to the addition of tests for other metabolic diseases. Over time, tests were added for endocrine disorders and now newborn screening program include more than 50 individual conditions.