D2I2.
genetic

Loeys–Dietz syndrome

Loeys–Dietz (LDS) is an disorder. It has features similar to Marfan syndrome and Ehlers–Danlos syndrome. The disorder is marked by aneurysms in the aorta, often in children, and the aorta may also undergo sudden dissection in the weakened layers of the wall of the aorta. Aneurysms and dissections also can occur in other than the aorta. Because aneurysms in children tend to rupture early, children are at greater risk for dying if the syndrome is not identified. to repair aneurysms is essential for treatment. It was previously believed that the life expectancy of an individual with this condition was around 30-40 years of age, however with progressive treatments such as possibilities for surgery and medications like Losartan it is proven now that life expectancy can be full age with the correct medical attention and scans.

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Plain-language summary adapted from Wikipedia. Not medical advice.