Last in a series. Read part one. Choosing genetic testing for Huntington’s disease is an act of courage on its own, as I pointed out in my column last week. […] The post A patient’s view of genetic testing for Huntington’s disease, part 2 appeared first on Huntington's Disease News.| Huntington's Disease News – The Web's Daily Resource for Huntington's Disea...
First in a series. When people ask my wife, Jill, about her Huntington’s disease, I never expect her reply to reach for a playground metaphor. But she has a way […] The post A patient’s view of genetic testing for Huntington’s disease, part 1 appeared first on Huntington's Disease News.| Huntington's Disease News – The Web's Daily Resource for Huntington's Disea...
When Tennille was first diagnosed with breast cancer, she had no idea it could have been connected to her grandfather’s prostate cancer.| Susan G. Komen®
Alnylam Act, a free genetic testing program, is now offering its services to certain patients in the U.S. and Canada suspected of having AHP.| Porphyria News
A recent study reveals a new variant of an intestinal virus found in a daycare worker. The discovery was accidentally made due to a lab error, which initially led to the mistaken diagnosis of bacterial meningitis.| epi.ufl.edu
The Information Commissioner’s Office (ICO) has fined a US genetic testing company £2.31 million under the UK GDPR following a 2023 cyber-attack. 23andMe provides genetic testing for, amongst…| Your Front Page For Information Governance News
With the explosion of genetic ancestry testing, more and more Americans are connecting with new parts of their ethno-racial identities. But does a White suburban New Yorker finding out they are 4% Cherokee make them Indigenous? If they believe it does, what are the implications for our everyday understandings of racial identity? A new article […]| Articles – Contexts
Breast cancer treatment isn’t one-size-fits-all. Personalized care is tailored to you. Learn more about tailored plans and treatment.| Susan G. Komen®
Carlos Briceño welcomes you to his new column, "A Family Tradition," where he discusses his family's journey with Huntington's disease.| Huntington's Disease News
Blood levels of two proteins, known as MMP9 and APP, could serve as biomarkers for fragile X syndrome where genetic testing is not possible.| Fragile X News Today