Campomelic Dysplasia is inherited in which pattern?

Campomelic Dysplasia is an autosomal dominant disorder, primarily caused by mutations in the SOX9 gene. This means that only one copy of the mutated gene inherited from an affected parent is sufficient to cause the condition in the offspring. The nature of the inheritance pattern is significant because it impacts family planning and genetic counseling for affected individuals and their families. In companies with autosomal dominant conditions, there's typically a 50% chance of passing the disorder to each child, which underscores the importance of understanding the inheritance pattern for risk assessment and management of the condition.