genetics
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Doctors Treated A Fatal Genetic Condition Before Birth
Nov 24
A team of doctors in the U.S. and Canada are reporting a medical first, Gizmodo reported. They were able to start treating a child’s rare and often deadly genetic condition while she was still a fetus in the womb - the same condition that claimed the lives of her siblings. Now 16 months old, the child, named Ayla, appears to be developing as...
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Embryos With DNA From Three People Develop Normally
Oct 20
A safety study published on Nature stated that researchers in China show that a technique used to replace diseased mitochondria does not affect early development. When the first baby to be conceived using a technique that mixes genetic material from three people was born in 2016, scientists worried that the procedure had not been studied to...
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Sharing Your 23andMe Health Report
Oct 11
After your 23andMe reports comes back, you might have questions about what to do next. When the question around a DNA result revolves around genetics and your health, that’s where a healthcare provider fits in. 23andMe reports can provide you with powerful information about health predispositions, pharmacogenetics, wellness, and more. Let...
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St. Jude Hospital Found Genetic Mutations In Cancer
Sep 22
Scientists from St. Jude’s Children’s Hospital have created a roadmap of the genetic mutations present in the most common childhood cancer, acute lymphoblastic leukemia (ALL). The St. Jude Children’s Research Hospital study is the first to supply a comprehensive view of the genomics of all subtypes of ALL. The work serves as a f...
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Oldest Case of Klinefelter Syndrome Discovered
Sep 15
Skull by Pixabay on Pexels Australian National University wrote that the oldest case of a rare genetic condition has been discovered in a 1,000-year-old skeleton from Portugal. Klinefelter syndrome gives men an extra X chromosome. What is Klinefelter Syndrome? Mayo Clinic explains that it is a genetic condition that results when a boy is bor...
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DNA Analysis Sheds Light On Victims Of 12th Century Violence
Sep 13
In 2004, workers on a construction site in Norwich, England, stumbled upon an 800-year-old well as they prepared the ground for a new shopping center. Inside the well, MyHeritage reported, they uncovered a heartbreaking and chilling sight: the remains of 17 people, including 6 adults and 11 children. A study titled: “Genomes from a medie...
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23andMe Launches Rare Disease Study
Sep 8
Listening to those with a rare disease, a common refrain is that they often feel isolated, unheard, and alone. But, they’re not alone, 23andMe says. Much to Learn While each rare disease is by definition uncommon - affecting fewer than 200,000 people - there are more than 7,000 known rare diseases. There are more than 300 million peopl...
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23andMe Announces A New Genetic Study On Pneumonia
Aug 25
23andMe announced that a new genetic study identified five regions in the human genome associated with susceptibility to pneumonia, a leading cause of death worldwide. Published in the journal Nature Communications, the study also found a surprising link between the risk of pneumonia and psychiatric conditions, such as schizophrenia, bipola...
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Mount Sinai Launches Genetics Project With Regeneron
Aug 23
Mount Sinai Health System and the Ichan School of Medicine at Mount Sinai have launched a new human genome sequencing research project called the Mount Sinai Million Health Discoveries Program with Regeneron Genetics Center (RGC), part of the industry-leading, New-York-based biotechnology company Regeneron. The Program aims to enroll o...
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Study On Side Effects of Parkinson’s Medication
Aug 11
23andMe posted information on a new genetic study that may help those looking for ways to avert some of the troubling side effects of a common medication used to treat Parkinson’s disease. Parkinson’s is sometimes treated with medication that increases dopamine activity in the brain. In some patients, that triggers impulsivity, such as ...