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Loeys-Dietz-Syndrom/en: Unterschied zwischen den Versionen

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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 aorta.
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Aneurysms and dissections also can occur in arteries 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. Surgery to repair aortic aneurysms is essential for treatment.
 
Aneurysms and dissections also can occur in arteries 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. Surgery to repair aortic aneurysms is essential for treatment.

Version vom 20. Juli 2019, 13:37 Uhr

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This syndrome shows similarities with Marfan syndrome and Ehlers-Danlos syndrome. Aneurysms of the aorta appear, often already in childhood. Due to the weak arterial wall, dissections of the aorta can also occur at an early age.

Aneurysms and dissections can also occur in other arteries. If the disease is not diagnosed early, children are in great danger because aneurysms tend to rupture more quickly in childhood.

https://en.wikipedia.org/wiki/Loeys%E2%80%93Dietz_syndrome ([1])


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Aneurysms and dissections also can occur in arteries 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. Surgery to repair aortic aneurysms is essential for treatment.