Cerebrocostomandibular Syndrome is a rare genetic disorder characterized by abnormalities in the development of the brain, ribs, and jaw. It is not contagious and cannot be transmitted from person to person. The syndrome is caused by genetic mutations and is typically present at birth. It affects various aspects of a person's physical and cognitive development. If you suspect that you or someone you know may have this syndrome, it is important to consult with a healthcare professional for proper diagnosis and management.
Cerebrocostomandibular Syndrome (CCMS) is a rare genetic disorder that affects the development of the brain, ribs, and jaw. It is characterized by various physical abnormalities, including intellectual disability, underdeveloped ribs, and a small jaw. CCMS is caused by mutations in the SF3B4 gene, which is involved in the production of proteins necessary for normal development.
CCMS is not contagious. It is a genetic disorder, meaning it is caused by changes in a person's genes and is not spread from person to person. The condition is typically inherited in an autosomal recessive manner, which means that both parents must carry a copy of the mutated gene for their child to be affected.
Although CCMS is not contagious, it is important to note that individuals with CCMS may have unique physical characteristics and developmental challenges. They may require specialized medical care and support to manage their symptoms and improve their quality of life. Early intervention and ongoing medical management can help individuals with CCMS reach their full potential and lead fulfilling lives.