ICYMI: Margo Gallegos, MS, CGC, recently spoke at the 2024 Advances in Autism Conference. Her presentation, "Precision Therapeutics in Profound Autism," explores how exome testing is a powerful tool that will drive future insights in autism and other pediatric-onset disorders. #exome #genetictesting #autism #VUS #PatientforLife https://hubs.ly/Q02D49MW0
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New eye-tracking biomarkers may help accelerate autism diagnosis, according to a new study published in Jama Network. For more information, visit: www.fratnow.com #autismandeyetracking #earlydiagnosis #eyetrackingbiomarkers #autismawareness #autismparenting #autismspectrumdisorder #asd #FRATtest #FRATAutism #FRAT #FRATNow
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The Nemechek Protocol® has produced many extraordinary clinical and anecdotal results over the past eight years. To gain perspective, in December 2022 we surveyed our mailing list and social media sites to quantify what parents have said. 71% of more than 700 respondents reported that The Nemechek Protocol® gains exceeded all other therapies tried. Specific improvements in Cognition, Communication, Speech, Anxiety & Aggression, and Socialization within just 6 months were shown. 83% of all users reported they planned to continue the protocol. See the survey results video. https://lnkd.in/dNtjkD_z (6 min) The Nemechek Protocol® reduces systemic inflammation by reversing bacterial overgrowth and rebalancing omega-3 and omega-6 fatty acids. The reduction in inflammation restores neurological pruning and repair mechanisms and often results in profound neurological gains within just a few months. Many protocol patients lose their ASD diagnosis and experience significant developmental improvements.
Improvements in Autism Using The Nemechek Protocol
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Our PGmaxTM - Intellectual Disability, Epilepsy, and Autism (IDEA) Panel is a good test to start with because intellectual disability (ID), epilepsy, and ASD have a high incidence of co-occurrence and significant overlap of genetic causes. https://ow.ly/p4jM50R3r8j
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Join us for our DUAL DIAGNOSIS OF DOWN’S SYNDROME AND AUTISM WEBINAR – PART ONE Thursday 11 April 2024 | 10:00 - 11:30 AM | £10 The first webinar is aimed at those who are wondering whether to pursue a diagnosis of autism. Register here 👉 https://loom.ly/bZbI1_0 #dualdiagnosis #webinar #autism
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An investigational eye-tracking device has identified a potential biomarker for autism spectrum disorder (ASD), as reported in 2 studies published by the Journal of the American Medical Association (JAMA). Although the majority of parents of children with ASD have concerns for their child’s development by age 2 years, the median age of diagnosis in the United States (US) is 4 to 5 years, and the delay is even longer for minority, low-income, and rural families. These delays pose major barriers to providing support and assistance at a developmentally sensitive time period. To aid in accurate and efficient diagnoses, researchers used an eye-tracking device, authorized by the U.S. Food and Drug Administration (FDA) for the development of an objective measurement of social visual engagement as a prospective biomarker of ASD. Read more: https://brnw.ch/21wFrVE #EyeTrackingDevice #PotentialBiomarkers #AutismSpectrumDisorder #ASD #Autism #AutismSpectrum #MedTech #SocialVisualEngagement #Biomarkers #Optometry #EyeCare #EyeHealth #PediatricOptometry
Eye-Tracking Test May Aid in Early Autism Diagnosis - Optometry Advisor
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🤚 𝗔𝗽𝗿𝗶𝗹 𝗶𝘀 𝗔𝘂𝘁𝗶𝘀𝗺 𝗔𝘄𝗮𝗿𝗲𝗻𝗲𝘀𝘀 𝗠𝗼𝗻𝘁𝗵! 🔵 𝗔𝘂𝘁𝗶𝘀𝗺 𝗶𝘀𝗻'𝘁 𝗰𝗮𝗹𝗹𝗲𝗱 𝗮𝗻 𝗶𝗹𝗹𝗻𝗲𝘀𝘀, 𝘀𝗼 𝘁𝗵𝗲𝗿𝗲'𝘀 𝗻𝗼 "𝗰𝘂𝗿𝗲." But tell that to a parent watching their child struggle every day—it's hardly reassuring. 𝗧𝗵𝗶𝘀 𝗶𝘀𝗻'𝘁 𝗰𝗼𝗺𝗳𝗼𝗿𝘁; 𝗶𝘁'𝘀 𝗻𝗲𝗴𝗹𝗲𝗰𝘁! 🔵 Every day, parents face an unbearable reality: Will my child get better, or will it only get harder? They deserve to know that experts are fiercely working towards solutions. 😡 𝗬𝗲𝘁, 𝘁𝗵𝗲 𝗽𝗵𝗮𝗿𝗺𝗮𝗰𝗲𝘂𝘁𝗶𝗰𝗮𝗹 𝗶𝗻𝗱𝘂𝘀𝘁𝗿𝘆’𝘀 𝗲𝗳𝗳𝗼𝗿𝘁𝘀 𝗮𝗿𝗲 𝗽𝗮𝗶𝗻𝗳𝘂𝗹𝗹𝘆 𝘀𝗹𝗼𝘄! 🔵 This isn't just a gap; it's a gaping hole in care. Autism rates are rising, but effective treatments aren't keeping pace. 🔵 The industry must prioritize autism research and treatment. We need to push for more. More understanding, more research, more solutions. It's time to call on the #pharmaceutical #industry to step up. We need them to do more for those living with autism. 🔵 𝗜𝘁'𝘀 𝘁𝗶𝗺𝗲 𝘁𝗼 𝗱𝗲𝗺𝗮𝗻𝗱 𝗮𝗰𝘁𝗶𝗼𝗻. For our children, for their future—we can't afford to wait. Let’s unite and push for change. Now! #autism #aprilisautimsawarenessmonth #autismawarenessmonth #pharmaindustry #biotechindustry #healthcare #medicine #genetic
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Explore our new blog on childhood developmental disorders. Understand the causes, symptoms, and treatments for conditions like Autism and Cerebral Palsy, and learn about potential breakthroughs, including umbilical cord blood transplantation that can revolutionise treatment options. Click here to read more: https://bit.ly/4bGWwf5 #lifecellin #stemcellbanking #umbilicalcord #umbilicalcordbloodbanking #ChildhoodDevelopment #developmentaldisorders #parentingtips #stemcell #braindevelopment #autismawareness #cerebralpalsy #cerebralpalsykids #parenthood #understandthecauses #treatmentplan #treatment
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Dr. Kurt Woeller and Dr. Sharon Hausman-Cohen discuss genetic variants that can affect individuals with autism and other special needs. In this unique webinar, they will go through a case where OATs testing, toxin testing, mitoswab, nutrient testing, and stool testing were all used with some improvement but then IntellxxDNA neurodevelopmental genomics was used to help this child cross the finish line. https://lnkd.in/eQvzEkf2
Genetic Variants That Can Affect Individuals With Autism and Other Special Needs
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According to a SPARK study, 74% of autism spectrum disorder (ASD) patients have at least one comorbidity, revealing the higher risks and complex diagnostic challenges of ASD. Whole Exome/Genome Sequencing (WES/WGS) can aid in a comprehensive diagnosis, informing medical management and improving outcomes. Learn more: https://lnkd.in/eiGAr4FZ #ThinkBG #Exome #Genome
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Today is Fragile X Awareness Day - a day where we celebrate individuals and families impacted by Fragile X and advocate for research, funding, and support. Fragile X is a genetic disorder that impacts brain development and can contribute to speech delays, intellectual disabilities, sensory issues, epilepsy, and more. Sharing this post helps spread the word about Fragile X and Fragile X Awareness Day, and the more people who know, the greater the support for those impacted. #fragilex #fragilexawarenessday
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