Congenital Myasthenic Syndrome (CMS) is a group of rare genetic disorders that affect the neuromuscular junction, the site where nerve cells communicate with muscles to control movement. This communication is […]
Tuberous sclerosis complex (TSC) is a genetic disorder that can affect various parts of the body, including the brain. It’s caused by mutations in either the TSC1 or TSC2 gene, […]
In today’s world, parents of children with developmental challenges often find themselves navigating a maze of medical appointments, tests, and treatments. For Sarah Foshee, a Florida mom, the journey began […]
While the exact causes of autism spectrum disorder (ASD) remain elusive, researchers have identified various factors contributing to its development, including both genetic and environmental influences. Among these, genetic factors […]
Autism Spectrum Disorder (ASD) presents as a perplexing neurodevelopmental condition marked by difficulties in social interaction, communication, and repetitive behaviors. Though the precise origins of ASD are not fully understood, […]
Receiving a diagnosis of autism spectrum disorder (ASD) is a pivotal moment in an individual’s life, shaping their journey toward understanding and support. Within the spectrum, there exist different levels […]
In the realm of neurodevelopmental disorders, epilepsy and autism spectrum disorder (ASD) stand as two distinct yet interconnected conditions. Their relationship is marked by complexities that researchers and healthcare professionals […]
Now offering Genetic Testing focused on Autism Autism Spectrum Disorder (ASD) is a complex neurodevelopmental condition that is believed to have both genetic and environmental factors contributing to its manifestation. […]
About 1 in 6 children are living with a developmental delay (DD), including autism spectrum disorder (ASD), Fragile X syndrome (FXS), and intellectual disabilities (ID). With such a high prevalence […]
Fragile X Syndrome (FXS) affects about 1 in 291 women and 1 in 855 men in the general population.[1] Women who carry fragile X mutations pass these mutations on to […]