First Genomix

First Genomix wishes you and your families a Happy #EidAlFitr. May the blessings of this occasion bring peace and joy to everyone.

"Autism Spectrum Disorders (ASD) comprise a range of complex neurodevelopmental conditions exhibiting diverse symptoms and severity levels, affecting social interaction and communication skills. Onset typically begins in early childhood, causing challenges in societal functioning. Both genetic and environmental factors may contribute to ASD. Genetic testing is pivotal in diagnosis as it allows tailored management strategies for affected individuals. For more information about #genetic #testing for #Autism Spectrum Disorders, call First Genomix on 04-3443222, or email info@firstgenomix.ae"

Tune it to the final part of our enlightening podcast where our guests share some real-life success stories about rare disease patients. They also aim to empower affected families, build hope, and offer them guidance through their journey. Watch the full episode on YouTube: https://lnkd.in/dMCrTfAx

What lies behind genetic testing? What makes it highly beneficial in the field of rare diseases? And how diverse is its use? Tune in to the third part of our podcast as our guests share valuable insights about genetic testing and its important applications within this critical health domain. Watch the full episode on YouTube: https://lnkd.in/dMCrTfAx

Diagnosing a rare genetic disease can be a challenging process if the correct diagnostic approach isn’t utilized. Tune in to the second part of this enlightening podcast with host Dany Mohsen, as our guests Dr. Ayman El Hattab and Sahar Abdelaziz highlight the most efficient technologies in genetic testing that can unravel the diagnostic mysteries underlying rare genetic diseases. Watch the full episode on YouTube: https://lnkd.in/dBAEfdPe

Join our host Dany Mohsen in this highly informative podcast about rare genetic diseases, featuring renowned guests Dr. Ayman El Hattab and Sahar Abdelaziz. Together, our genetic experts will shed light on this under-discussed yet highly pressing topic, uncovering aspects that are commonly unknown and offering valuable insights to affected families and clinicians. Watch the full episode on YouTube: https://lnkd.in/dBAEfdPe . . . #RareDiseases #GeneticDisorders #HealthPodcast #Genetics #ScienceTalk #HealthAwareness

From our team members at First Genomix, we extend our heartfelt wishes to all #mothers, in appreciation of their selfless devotion and the boundless #love they shower upon their #families. #happymothersday #mothersday2024

Rare genetic disorders often come with subtle or nonspecific symptoms, making early diagnosis difficult. Genetic testing is a pivotal step that facilitates the early and accurate diagnosis of such disorders. Whole Exome Sequencing from First Genomix, is a specialized test driven by highly advanced NGS technology that scans the body’s more than 20,000 genes, to identify abnormal genetic changes that drive disease. For more information on WES, contact First Genomix at 04-3443222, or email us at info@firstgenomix.ae #raregeneticdisorders #raregeneticdisease #earlydiagnosis #ngstechnology #genes #geneticchanges

Children are the world’s greatest asset, and it’s our responsibility to ensure that they have the best chance of being born healthy. As per the ACMG, all couples are highly recommended to perform Carrier Screening to assess their risk of passing on genetic abnormalities to their future children. To book your Carrier Screening test, contact First Genomix on 04-3443222, or email us at info@firstgenomix.ae Test today for a healthier tomorrow! #diseasetransmission #diseasetransfer #ACMG #childrenhealth #childrenfuture #genetictesting #carrierscreening

Wishing everyone a blessed and peaceful #Ramadan. May the holy month fill your hearts with serenity and gratitude.