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Loeys–Dietz syndrome (LDS) is an autosomal dominant genetic connective tissue 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…
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syndrome loeys dietz aneurysms aortic marfan losartan identified aorta may also disorder cause surgery mutations condition autosomal patients features risk
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Loeys–Dietz syndrome | Other names | Aortic aneurysm syndrome due to TGF-beta receptors anomalies | 1.00 | infobox |
| Loeys–Dietz syndrome | Pronunciation | /ˌloʊiːzˈdiːts/ LOH-eez-DEETS | 1.00 | infobox |
| Loeys–Dietz syndrome | Specialty | Cardiology, rheumatology, medical genetics | 1.00 | infobox |
| Loeys–Dietz syndrome | is a | lifelong condition | 0.90 | text |
| possibilities for surgery | instance of | however with progressive treatments | 0.80 | text |
| medications like Losartan it is proven now that life expectancy can be full age with the correct medical attention | instance of | however with progressive treatments | 0.80 | text |
| scans.There are five types of the syndrome | instance of | however with progressive treatments | 0.80 | text |
| designated types I through V | instance of | however with progressive treatments | 0.80 | text |
| caused by mutations in TGFBR1 | instance of | however with progressive treatments | 0.80 | text |
| TGFBR2 | instance of | however with progressive treatments | 0.80 | text |
| SMAD3 | instance of | however with progressive treatments | 0.80 | text |
| TGFB2 | instance of | however with progressive treatments | 0.80 | text |
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