Greig Cephalopolysyndactyly Syndrome (GCPS) is a rare genetic disorder characterized by multiple physical abnormalities, including extra fingers or toes, fused or webbed digits, and craniofacial anomalies. It is important to note that GCPS is not contagious as it is caused by mutations in specific genes. It is inherited in an autosomal dominant pattern, meaning that a child has a 50% chance of inheriting the syndrome if one parent carries the mutated gene. GCPS is a genetic condition and cannot be transmitted from person to person.
Greig Cephalopolysyndactyly Syndrome (GCPS) is a rare genetic disorder that affects the development of the limbs and skull. It is caused by mutations in the GLI3 gene and is typically inherited in an autosomal dominant manner, meaning that an affected individual has a 50% chance of passing the condition on to their children.
GCPS is not contagious in the traditional sense. It is not caused by a virus or bacteria and cannot be transmitted from person to person through contact or exposure. Instead, it is a genetic condition that is present from birth and is typically inherited from a parent who also has the syndrome.
Individuals with GCPS may exhibit a range of symptoms, including fused fingers or toes (syndactyly), extra fingers or toes (polydactyly), and abnormalities in the shape of the skull and face. These physical characteristics are a result of disrupted embryonic development.
While GCPS itself is not contagious, it is important to note that the genetic mutation responsible for the syndrome can be passed on to future generations. Genetic counseling and testing are recommended for individuals with GCPS or a family history of the condition to better understand the risks and make informed decisions about family planning.