→ Cornelia de Lange Syndrome

→ Cornelia de Lange Syndrome

Back to Previous Cornelia de Lange Syndrome Cornelia de Lange syndrome (CdLS) is a rare genetic disorder that is generally apparent at birth (congenital). Associated symptoms and findings typically include delays in physical development before and after birth...
→ Cornelia de Lange Syndrome

→ Creatine Transporter Deficiency

Back to Previous Creatine Transporter Deficiency Creatine transporter deficiency (CTD) is an inborn error of creatine metabolism. The onset of symptoms occurs during infancy, but the average age of diagnosis ranges from 2 to 66 years of age. Since the disease is now...