Syndromes/Craniofacial Anomalies
The purpose of this case report is to present a pediatric patient with Ehlers-Danlos Syndrome and document the dental management. Ehlers-Danlos syndrome is a genetic condition that affects the body’s connective tissue. There are thirteen major types of Ehlers-Danlos Syndrome, and each type affects a different area of the body. Symptoms of classic Ehlers-Danlos syndrome may include heart valve problems, benign growths on elbows and knees, muscle fatigue, muscle pain, redundant skin folds on the eyes, skin that bruises easily, fragile skin, high elastic and velvety skin, and loose joints. Echocardiogram, skin biopsy, and genetic tests may be used to diagnose Ehlers-Danlos syndrome. Treatment may include drugs to decrease pain, surgery to fix damaged joints, and physical therapy. A case report of a 5-year-old-male with Ehlers-Danlos syndrome is presented along with other medical conditions.