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Updated: Feb 26, 2026

06:41
In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
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[Loeys-Dietz Syndrome, 3 generations, 4 familial cases]
Carlos F Rosental1, Silvina Neiling1, Natalia Napoli2
1Hospital General de Pediatría "Prof. Dr. Juan P. Garrahan". Ciudad Autónoma de Buenos Aires.
Archivos Argentinos De Pediatria
|July 25, 2017
Abstract:
Loeys-Dietz Syndrome is an autosomal dominant disease with aortic aneurysms, arterial tortuosity with hypertelorism and bifid uvula. We describe four familial cases within three generations. The diagnosis, surgical management and followup will be addressed.
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