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
From: Wikipedia: Loeys-Dietz Syndrome
Sites 6
Loading new listings for you to review...
- Loeys-Dietz Syndrome Information in this brief Wikipedia article includes symptoms, treatment, and additional links.
- Loeys-Dietz Syndrome MedicineNet explains what it is, signs and symptoms, inheritance factors, causes, diagnosis, and treatment. Includes glossary and link to the Loeys-Dietz Syndrome Center.
- Largest Review of Loeys-Dietz Syndrome To Date 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.
- Loeys Dietz Syndrome Foundation Explains the syndrome and the mission of the foundation. Includes medical information and resources.
- Loeys Dietz Syndrome Information from Johns-Hopkins Heart and Vascular Institute covers definition, symptoms, diagnosis, and complications.
- OMIM - Loeys-Dietz Syndrome Offers a history of the discovery of LD syndrome, including similarities and differences to previously-known syndromes.