Loeys-Dietz syndrome is a recently-discovered autosomal dominant genetic syndrome which has many features similar to Marfan syndrome, but which is caused by mutations in the genes encoding transforming growth factor beta receptor 1 (TGFBR1) or 2 (TGFBR2). It was identified and characterized by American physician Harry C. Dietz and Belgian physician Bart L. Loeys, for whom it is named. From: Wikipedia: Loeys-Dietz Syndrome- Category ID : 75931
MedicineNet explains what it is, signs and symptoms, inheritance factors, causes, diagnosis, and treatment. Includes glossary and link to the Loeys-Dietz Syndrome Center.
Provides comparison of symptoms between LD syndrome and Marfan syndrome, to improve diagnoses. Includes physical characteristics, symptoms, course of disease, gene analysis, and timing and effect of treatment.