No cure; management focuses on addressing specific symptoms and improving quality of life
Cleidocranial dysostosis is a rare genetic disorder characterized by skeletal abnormalities, including delayed closure of the skull bones and collarbone abnormalities. Treatment may involve surgical interventions to address specific issues.
Rare genetic disorder affecting the development of bones and teeth, particularly the collarbones and skull
Abnormalities in collarbones, delayed closure of fontanelles, dental abnormalities
Clinical evaluation, genetic testing, sometimes imaging studies
Variable, depends on the specific features and complications
Dental abnormalities, bone deformities, complications affecting multiple systems
Genetic mutations affecting the RUNX2 gene
Management of symptoms, orthodontic and dental care, surgical interventions in some cases
Management of symptoms, orthodontic and dental care, surgical interventions in some cases
Genetic disorder affecting bone and tooth development, characterized by open fontanelles and other features
Supportive care, management of associated conditions
This information is for general understanding and is not a substitute for professional medical advice. Always consult with healthcare providers for accurate and personalized information related to your health.
Share: