Townes–Brocks syndrome
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Townes–Brocks syndrome[1] (TBS) is a rare genetic disease that has been described in approximately 200 cases in the published literature. It affects both males and females equally.[2] The condition was first identified in 1972.[2] by Philip L. Townes, who was at the time a human geneticists and Professor of Pediatrics, and Eric Brocks, who was at the time a medical student, both at the University of Rochester.
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Townes–Brocks syndrome | |
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This condition is inherited in an autosomal dominant manner | |
Specialty | Medical genetics |
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