Li-Campeau Syndrome (LICAS)

Li-Campeau Syndrome, also known as licas, is related to cerebellar atrophy, developmental delay, and seizures. An important gene associated with Li-Campeau Syndrome is UBR7 (Ubiquitin Protein Ligase E3 Component N-Recognin 7). Affiliated tissues include brain, and related phenotypes are intellectual disability and global developmental delay