National Society of Genetic Counselors

Big news for 2025! 🎉 The new CPT Code 96041 goes into effect January 1, and it’s a game-changer for genetic counseling. Hear from COLLEEN CAMPBELL as she talks about the new code on the DNA Today podcast! https://lnkd.in/gVVVERXH

Discover the future of prenatal genetic screening with Myriad Genetics this January! Join us for a webinar on fetal fraction amplification and AMPLIFY™ technology, revolutionizing Cell-Free DNA screening for aneuploidy and genetic conditions. Explore advancements like expanded aneuploidy analysis, earlier gestational age screening, and more. Don’t miss out—register today! #sponsored 🔗 : https://lnkd.in/gDJ9YyAM

Can AI help interpret NCCN guidelines for hereditary cancer testing? This #Perspectives article weighs the pros, cons and lessons from tools like ChatGPT and ClaudeAI. Read more: https://lnkd.in/gMywwHwF #GeneChat

Hypotonia, dystonia, developmental delay with severe weight loss and other symptoms of thyrotoxicosis? Could it be MCT8 deficiency? MCT8 deficiency, also known as Allan-Herndon-Dudley syndrome, is a rare, X-linked genetic disorder caused by mutations in the SLC16A2 gene that encodes the thyroid hormone transporter, monocarboxylate transporter 8 (MCT8). If your patient has MCT8 deficiency, learn more about the ReTRIACt study aiming to assess the safety and effectiveness of an investigational drug in treating MCT8 deficiency. Enrollment is open for males aged 4 and up, with study sites enrolling in Georgia, North Carolina, Texas and Pennsylvania. For more information, visit www.mct8deficiency.com or email Recruit@retriact.egetis.com. #AdvanceResearch4MCT8 #Sponsored

Direct-to-consumer genetic testing can reveal unexpected parentage, reshaping the test taker's identity and family ties. A new #JoGC study highlights grief, strained bonds and newfound connections. Dive into the findings: https://lnkd.in/gUZCGJgf #GeneChat

The Call for Sessions is open for the NSGC 44th Annual Conference in Seattle! Submit your ideas on key topics like cancer genetics, AI, patient stories & more, or nominate a speaker for the Janus Lecture! 📆 Deadline: Jan. 31, 2025 Learn more: https://lnkd.in/guqZSUCR #GeneChat

Attention, genetic counselors! As the new CPT Code takes effect next month, stay informed about how these updates may impact your practice. Visit https://lnkd.in/grihtvKN for resources and guidance on navigating the changes. #GeneChat

We're thrilled to welcome Rachel Mills, one of NSGC's Incoming Directors-at-Large, to the 2025 Board of Directors! 🎉 Rachel brings a wealth of knowledge and a passion for advancing the genetic counseling profession. Swipe to learn more about her vision for the future of NSGC. #GeneChat

New research highlights the importance of empathetic disclosure and comprehensive support for those with XXY (Klinefelter syndrome). Gaps in healthcare, the impact of stigma on self-identity, and the critical need for thoughtful, age-appropriate communication are just a few insights. Addressing psychosocial needs and providing interdisciplinary care can empower individuals and improve their well-being across the lifespan. Explore the findings in this #JoGC article: https://lnkd.in/gShCRd84 #GeneChat

Celebrate #NationalFamilyHealthHistoryDay this #Thanksgiving by gathering important health information when you’re with your loved ones. To learn more about how to keep track of your family’s health history, swipe through and visit our website: https://bit.ly/4g8pCoK ➡️ #GeneChat