Loeys-Dietz Syndrome
New loeys-dietz syndrome research from J.T.L. Choo et al outlined
Published in Cardiovascular Week, December 28th, 2009
According to recent research from Singapore, Singapore, "Loeys-Dietz syndrome is a recently-characterised genetic disorder with an autosomal dominant inheritance due to mutations in the transforming growth factor beta-receptor Type 1 or Type 2 genes. We present a Chinese female neonate with genetically-confirmed Loeys-Dietz syndrome, cleft palate, hypertelorism, and an early dilatation of the aortic root and ascending aorta."
"This syndrome is associated with an aggressive arteriopathy, with an increased risk of dissection and rupture. Early diagnosis, close monitoring and early surgery may prolong the life in affected individuals," wrote J.T.L. Choo and...
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Source: Cardiovascular Week (2009-12-28)
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