Claria Webinar - Prenatal 22q11.2 Deletion Syndrome and Microdeletions Screening скачать в хорошем качестве

Claria Webinar - Prenatal 22q11.2 Deletion Syndrome and Microdeletions Screening

Explore the significance of Claria Webinar on Prenatal 22q11.2 Deletion Syndrome and Microdeletions Screening in advancing prenatal care. This session delves into the role of genetic testing in identifying 22q11.2 deletion syndrome and other microdeletions, which are critical for understanding fetal health during pregnancy. Learn how advanced screening techniques, including chromosomal microarray and other innovative methods, aid in detecting these genetic conditions early, empowering parents and healthcare providers to make informed decisions. Gain valuable insights into the importance of microdeletions screening and how it contributes to better outcomes in prenatal he ▬⏰⏰ Contents of this video ⏰⏰ ▬▬ 0:00 Claria 2:41 The Evolution of Prenatal Genetic Screening 5:18 ISPD-microdeletions 8:31 Repeats can affect the alignment 11:05 Congenital Cardiac Anomaly 11:44 Developmental delay in pre-school children 12:26 Opportunities for early intervention in developmental delay 12:49 22q11 and absence of the thymus 13:51 Prenatal screening and testing involves uncertainty 14:43 Why do we do prenatal screening? 15:09 22q11 syndrome 15:54 Important ethical considerations for 22q11 17:03 22q11 case studies 20:25 Sensitivity in validation study 22:30 Continuous improvements in test performance 23:56 Guidelines in 2016 ACMG Statement: Pretest Counseling 25:26 Guidelines in 2016 ACMG Statement: Post-test Counseling 27:41 The evolution of NIPT 28:25 Summary - NIPT for 22q11.2 deletion syndrome 30:59 22q11 clinical sensitivity and specificity--------------------------------------------- 🩺Book Genetic Counseling session with our experts here: https://diagnostics.medgenome.com/ ✅Explore Our Resources: Blogs: https://diagnostics.medgenome.com/blog/ Patient Stories: https://diagnostics.medgenome.com/pat... Press Media Mentions: https://diagnostics.medgenome.com/press/ 👍Follow and Like us on: Instagram:   / medgenome   Facebook:   / medgenomelabs   Twitter: https://x.com/medgenomelabs LinkedIn:   / medgenomelabs   🤝Connect With Us: Email: [email protected] Toll-free number: 1800 296 9696 ⬇️Download Our Application: Android: https://bit.ly/3yYVvAb iOS: https://bit.ly/4cxRikU #PrenatalScreening #22q11DeletionSyndrome #MicrodeletionsScreening #GeneticTesting #PrenatalCare #ChromosomalMicroarray #MicrodeletionsTest #FetalHealth #ClariaWebinar #PrenatalDiagnosis --------------------------------------------- About MedGenome MedGenome is a global leader in genetic testing services, genomics research, and drug discovery solutions. Since 2013, we have been committed to delivering world-class genomic solutions with precision and accuracy, empowering every individual to manage their health better. We are proud to be the only CAP-accredited genetic testing lab in India, offering 1300+ genetic tests backed by the latest and most advanced technologies available worldwide. MedGenome is dedicated to providing the best precision testing solutions for quicker and smarter diagnosis of complex diseases. Our Mission We are on a mission to democratize access to quality and affordable genetic solutions, serving over 4 billion people for their healthcare needs through the power of genetic testing. Our Expertise We operate Southeast Asia's largest CAP-accredited Next Generation Sequencing (NGS) lab, equipped with cutting-edge genome sequencing platforms such as Illumina’s NovaSeq, HiSeq X, MiSeq, and more. Our team consists of expert molecular biologists, geneticists, data scientists, and bioinformaticians driving our genomics research. As a firm believer in quality, MedGenome adheres to the highest international standards in our services and has obtained the prestigious CAP accreditation for our main lab in Bangalore. At MedGenome, we continue to push the boundaries of genetic research, providing insights into complex diseases and driving innovation in personalized medicine. --------------------------------------------- Disclaimer: The content provided in this video is intended solely for educational purposes. It should not be used as a substitute for professional medical advice, diagnosis, or treatment. If you have any concerns, please consult a qualified healthcare provider. MedGenome accepts no liability for individual interpretations of the content, although it is accurate to the best of our knowledge at the time of publication.