Dietz Syndrome Loeys Genetic Disorders
Dietz Syndrome Loeys Genetic Disorders
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
Top: Health: Conditions and Diseases: Genetic Disorders: Loeys-Dietz Syndrome
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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.
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OMIM - Loeys-Dietz Syndrome - Offers a history of the discovery of LD syndrome, including similarities and differences to previously-known syndromes.
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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.
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Loeys Dietz Info Board - Follow the history of one patient. Includes news, signs and symptoms, research, personal pages, and medical centers.
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