Burkitt's connective tissue disorder

Burkitt's connective tissue disorder is a rare genetic condition where the body's connective tissues—such as skin, muscles, and bones—develop abnormally, leading to symptoms like joint problems, weak skin, and growth issues. It is caused by mutations affecting how the body produces connective tissue components like collagen. These abnormalities can result in increased fragility of tissues, delayed healing, or unusual tissue growth. While it primarily affects growth and tissue strength, the severity and specific symptoms can vary among individuals. Diagnosis typically involves genetic testing, and management focuses on addressing symptoms and improving quality of life.