Marfan syndrome's features were systematically described ... "The new findings could help us better understand why the aortic root is likely to dilate in patients with Loeys-Dietz syndrome ...

Marfan syndrome is a rare genetic condition ... Most critically, both of our children present with aortic root dilation, and they daily take an adult blood pressure medication that is compounded ...

Objective To construct an adjusted nomogram for the echocardiographic screening of aortic root diameter in children ... undergoing Marfan screening from 1983 until 1996, the diagnosis Marfan syndrome ...

In 1896 Antoine Marfan ... and the adoption of this as a syndrome was based upon these characteristic phenotypic appearances. Autosomal dominant inheritance was recognised in 1931. The first ...

In specific populations, including those with Marfan syndrome and Loeys–Dietz syndrome, descending thoracic aortic aneurysm can grow at accelerated rates and likely warrant closer imaging surveillance ...

NEW YORK—Streaming tech provider ViewLift has announced the launch of the new Root Sports Stream app that deliveres Seattle Mariners games and Root Sports programming directly to fans across the ...

Loeys-Dietz syndrome (LDS), caused by mutations in the TGF-β (transforming growth factor-β) signaling cascade, leads to aggressive thoracic aneurysms. While vascular smooth muscle cell (SMC) phenotype ...

Bartter syndrome is a group of similar rare conditions that affect the kidneys. It's genetic, meaning it's caused by a problem with a gene. If you have this condition, too much salt and calcium ...

It is important to identify infants of affected women as high-risk infants. Scrutinize the maternal history and, when possible, determine the specific EDS type of the mother or affected family ...

The following is a summary of "A new guiding strategy for treating the free margin of the leaflet in an aortic root remodelling procedure,” published in the March 2025 issue of the Journal of ...