Newborn screening

Genetics Testing Introduction to Genetic Testing Genetic testing, also known as DNA testing, is the process of using medical tests used to look at one’s genes, inherited from one’s parents. These tests ranges from identifying a child’s biological parents, to ascertaining if there are any risks of having cancer or diseases. Results of genetic testing may help access on how severe a disease might be and find the best solution to diagnose it. It will also help determine the chances of developing…

therapy and tutoring and Advocacy for children who are “stuck”. As the foster families of Mother’s choice play a crucial role in ensuring that a child receives the best care during his/her stay with Mother’s Choice. Mother’s Choice conducts a thorough screening of each foster family to ensure that the home meets the needs of the foster child. They empower our foster parents to create an enriching environment for children through Regular training and workshops and Support groups and mentorship.…

Hearing is a complex process where thousands of tiny hair cells, located in the cochlea of the ear, convert vibrations of sound waves into electrical nerve pulses. These pulses are understood by the brain to be what a person hears as sound. Hearing loss can occur throughout any part of the ear, and in varying degrees of severity. As hearing loss can affect a child’s ability to develop speech, language, and social skills, it is important to identify any signs and symptoms early in the child’s…

sick.” So, preexisting conditions are not a barrier anymore to insurance, including high-risk customers. Your treatment cannot cost more because of your health status. There are no co-pay for routine check ups, physicals, immunizations and cancer screenings. Insurers are prohibited from dropping policyholders when they get sick. Before ObamaCare, people with illnesses, such as cancer, diabetes, hypertension, high cholesterol, etc, made it harder for people to get insurance. Insurance companies…

Cystic fibrosis is a severe, but rare genetic condition. It usually surfaces at a young age and affects lungs and the digestive system in which mucus builds up. The Cystic Fibrosis Foundation reported roughly 70,000 cases worldwide. Patients with this condition are predisposed to infections by Pseudomonas aeruginosa. This bacteria causes infections in the lungs as it favors conditions with large amounts of mucus, typical for cystic fibrosis patients. The bacteria adapts and grows in this unique…

It is important for a woman trying to conceive later in life to go to a specialized obstetrician for a variety of tests that can check for chromosomal abnormalities. In the first trimester, a screening test can be done at 12 weeks. This will include a blood test, as well as an ultrasound where doctors look for something called a nuchal translucency. If the stripe is thin and the blood test is normal, there’s a very good chance that the baby is…

of the disorder. Prenatal genetic screening concentrates on personal decision making compared to supervision of analytic disease. Positive screenings conclude more specific tests to justify condition in embryo. There is no treatment available for majority of the conditions before birth. This causes possibility of pregnancy termination by couples or women resulting in ethical dilemma as those who don’t make these decisions can desire to not have prenatal screening. For those conditions with no…

because they know what it's going to be like when the baby come. They won't just be give a baby with a disease they know nothing about, while having to try and raise him/her. “In other cases, expecting parents may use information from prenatal screening and diagnosis to plan for their baby’s care (Prenatal…

I Want to Be a Human Geneticist Every feature on your body has a story behind it —from the color of your hair and skin, to all your moles and freckles. It is the job of a human geneticist to uncover these stories under the microscope. Hunan geneticists have amazing abilities. They can tell you why some of your features are similar to your parents and other relatives, or why you have allergies. They can also trace where your ancestors came from based on a small sample of your blood, hair, or…

from. This is used for people who already have signs of a disease. Carrier testing will tell you if you are a carrier and if you will pass it on to your offspring, and is offered to people who have a family history of a certain disease. Newborn screening is for newborns one to two days old, and it determines whether that infant has certain diseases. Pharmacogenomic testing gives information about how certain medicines are processed by an individual's body. This type of testing can help your…