GENETIC TESTING

Advertisement
Jan 06 2026HEALTH

Family Health Mystery: The Hidden Gene Link to Weight Gain

A family spanning four generations has uncovered a surprising health secret. A genetic test on a young child revealed a mutation in the MC4R gene. This gene is linked to weight gain and obesity. The same mutation was also found in three older relatives. This discovery came after years of struggling

reading time less than a minute
Dec 26 2025HEALTH

Smart Medicine: How Gene Testing Could Save Lives and Money in Thailand

Healthcare in Thailand might get a big upgrade with a new idea called pharmacogenetic (PGx) testing. This test looks at a person's genes to figure out the best medicine for them. It's like a roadmap for doctors to pick the right treatment. Right now, doctors in Thailand often give a medicine called

reading time less than a minute
Nov 23 2025HEALTH

Speeding Up Care: How Quick DNA Tests Could Save Tiny Lives

In the world of medicine, time is often of the essence, especially when it comes to the tiniest patients. Newborns in the neonatal intensive care unit (NICU) often need swift and accurate diagnoses to guide their treatment. Traditionally, DNA testing has been a slow process, taking days to complete

reading time less than a minute
Jul 20 2025HEALTH

How Docs Without Genetics Training Can Help Patients

Doctors who aren't genetics experts might soon play a bigger role in genetic testing. Why? Because there's a huge need for these tests, but not enough geneticists to go around. This is making healthcare systems struggle to keep up. The idea is to train other doctors to handle some of these tests. T

reading time less than a minute
Jul 04 2025HEALTH

Parents' Views on Genetic Testing for Kids with Rare Neurological Issues

Parents of children with rare neurological disorders have a lot to think about when it comes to clinical genetic testing (CGT). A recent study asked 101 parents about their thoughts on this topic. The children involved had conditions like cerebral palsy, epilepsy, and developmental delays. Most par

reading time less than a minute
Jul 01 2025HEALTH

A New Chapter for 23andMe: What's Next for Your Genetic Data?

A big change is happening for 23andMe. A court just gave the green light for the company to be sold to a nonprofit group. This group is led by Anne Wojcicki, who used to be the CEO. The sale is worth $305 million. This is not the first time 23andMe has been up for sale. Earlier, there was a $256 mil

reading time less than a minute
Jun 20 2025SCIENCE

How Beliefs Shape Our Views on Genetic Research

Genetic research has become a hot topic in recent years. It is a field that holds immense potential for medical advancements. However, public opinion on this subject is not uniform. It is influenced by a variety of factors. One of the most significant factors is religion. This is according to a

reading time less than a minute
Jun 05 2025HEALTH

Why Aren't More People Getting Genetic Cancer Tests?

Genetic testing for cancer is a powerful tool that can spot cancer risks early. But, surprisingly, not many people are taking advantage of it. A recent investigation dug into why this is happening. It looked at how a person's role as a caregiver, their involvement in online support groups, and their

reading time less than a minute
May 19 2025HEALTH

Latino Communities and Genetic Testing: What Drives Their Decisions?

Genetic testing has been a hot topic in health circles for years. However, not much thought has gone into how different communities view it. This is especially true for Latino groups. Researchers have looked at attitudes and clinical processes. Yet, they often miss out on using helpful theories. One

reading time less than a minute
May 12 2025HEALTH

The Knowledge Gap: How Well Do Doctors Know About Fragile X Syndrome?

Fragile X syndrome (FXS) is a condition that often leads to developmental delays, intellectual disabilities, and autism spectrum disorder. Since 2016, genetic testing for FXS has been part of Japan's national health insurance. Despite this, the number of FXS diagnoses remains surprisingly low. This

reading time less than a minute