FAM109B
Blog Post: FAM109B: Unveiling the Mysteries of a Gene Linked to Neurodevelopmental Disorders
Description:
FAM109B, an enigmatic gene located on chromosome 1, has recently emerged as a genetic player linked to a range of neurodevelopmental disorders. These disorders affect brain development and function, leading to challenges in communication, socialization, and mobility. FAM109B has sparked the interest of researchers as it appears to be involved in several neurodevelopmental processes, including cell migration, synaptic plasticity, and neuronal communication.
Associated Diseases:
Recent studies have associated mutations or variations in the FAM109B gene with various neurodevelopmental disorders, including:
- Autism spectrum disorder (ASD)
- Intellectual disability (ID)
- Developmental delay
- Language impairment
- Motor coordination difficulties
- Attention deficit hyperactivity disorder (ADHD)
Did you Know ?
Studies have estimated that FAM109B mutations account for approximately 1% of cases of ASD and a smaller percentage of cases of other neurodevelopmental disorders. However, researchers believe that its true contribution may be underestimated due to its complex genetic interactions and phenotypic heterogeneity.
