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Neuroradiologic manifestations of Loeys-Dietz syndrome type 1. (1/23)

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Loeys-Dietz syndrome type I and type II: clinical findings and novel mutations in two Italian patients. (2/23)

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Loeys-Dietz syndrome: a Marfan-like syndrome associated with aggressive vasculopathy. (3/23)

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. Losartan is an emerging therapy that may help slow down the rate of arterial dilatation.  (+info)

Glue embolus complicating the endovascular treatment of a patient with Loeys-Dietz syndrome. (4/23)

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Valve-sparing aortic root replacement in children: intermediate-term results. (5/23)

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Dexamethasone normalizes aberrant elastic fiber production and collagen 1 secretion by Loeys-Dietz syndrome fibroblasts: a possible treatment? (6/23)

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Management of pregnancy in patients with congenital heart disease. (7/23)

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Familial aortic aneurysm and dissection due to transforming growth factor-beta receptor 2 mutation. (8/23)

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