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PedAM

Pediatric Disease Annotations & Medicines




Disease aneurysm
Phenotype C0024796|marfan syndrome
Sentences 30
PubMedID- 25096902 Impact of aortic aneurysm on hospitalizations in patients with marfan syndrome: a multi-institutional study.
PubMedID- 22794337 Modified "stent-graft sandwich" technique for treatment of isolated common iliac artery aneurysm in patient with marfan syndrome.
PubMedID- 19879959 We have described that the progression of thoracic aortic aneurysm in marfan syndrome is accompanied with aortic vascular dysfunction.
PubMedID- 23359416 Should aortic arch replacement be performed during initial surgery for aortic root aneurysm in patients with marfan syndrome.
PubMedID- 23407346 Giant aortic aneurysm in marfan syndrome.
PubMedID- 24378247 Axillary arterial aneurysm associated with marfan syndrome is an extremely rare and dangerous disease because of its potential risk for rupture and impairment of neurologic function in the upper extremities.
PubMedID- 21039445 Results: serum fetuin-a levels (median and iqr) were significantly lower in the atherosclerotic aneurysm cohort than in patients with marfan syndrome: 708 mug ml(-)(1) (612-780) and 756 mug ml(-)(1) (708-816), respectively, (p = 0.0428).
PubMedID- 21532308 A huge noncoronary sinus of valsalva aneurysm in a patient with marfan syndrome.
PubMedID- 20333568 Valve-sparing operation for aortic root aneurysm in patients with marfan syndrome.
PubMedID- 26403341 Background: in many cardiac units, aortic valve-sparing operations have become the preferred surgical procedure to treat aortic root aneurysm in patients with marfan syndrome, based on relatively short-term outcomes.
PubMedID- 26123456 This is the first case of gastric artery aneurysm described in a patient with marfan syndrome.
PubMedID- 20340073 As far as we know, this is the first description of a hand aneurysm in a patient with marfan syndrome.
PubMedID- 22321477 Modified "stent-graft sandwich" technique for treatment of isolated common iliac artery aneurysm in patient with marfan syndrome.
PubMedID- 21168034 Giant aortic root aneurysm in marfan syndrome: a rare complication in early childhood.
PubMedID- 21228428 Context: surgical treatment of aortic root aneurysm in marfan syndrome (mfs) patients.
PubMedID- 20643034 To report a technique to maintain pelvic flow to an internal iliac artery (iia) with aneurysm in a patient with marfan syndrome, and previously treated by infrarenal abdominal aortic aneurysm open procedure.
PubMedID- 22156153 Fenestrated endograft repair of suprarenal aortic patch aneurysm in a patient with marfan syndrome.
PubMedID- 21317477 Dissecting aortic aneurysm with marfan syndrome.
PubMedID- 20871099 Differential effects of alendronate and losartan therapy on osteopenia and aortic aneurysm in mice with severe marfan syndrome.
PubMedID- 25216402 Pelvic pain from a giant presacral tarlov cyst successfully obliterated using aneurysm clips in a patient with marfan syndrome.
PubMedID- 26494287 Genetic analysis of the contribution of ltbp-3 to thoracic aneurysm in marfan syndrome.
PubMedID- 22818967 Methods: from october 1999 through july 2011, 20 consecutive patients with marfan syndrome underwent repair of dissecting aneurysm of the thoracoabdominal aorta (median age, 45 years; range, 19-65 years).
PubMedID- 22477577 Large pulmonary artery aneurysm associated with marfan syndrome.
PubMedID- 23496804 Exclusion criteria were: (i) marfan syndrome or history of familial aortic aneurysm, (ii) internal ascending aortic diameter greater than 4.5 cm based on echocardiographic measurements, (iii) left ventricular ejection fraction <55%, (iv) moderate or severe aortic stenosis, (v) moderate or severe aortic regurgitation, (vi) aortic valve replacement, (vii) aortic coarctation, and (viii) blood pressure >160/90 mmhg.
PubMedID- 23977594 Syndromic aneurysms have been associated with marfan syndrome, loeys-dietz syndrome, aneurysm osteoarthritis syndrome, arterial tortuosity syndrome, ehlers-danlos syndrome, and tgfbeta mutation.
PubMedID- 21315290 Aortic aneurysm can result from both marfan syndrome (mfs) and hypertension.
PubMedID- 24442477 Importantly, the aneurysm in marfan syndrome develops preferentially in the ascending aorta and arch, regions that develop from neural crest and perhaps secondary heart field.
PubMedID- 26506064 Furthermore, patients with marfan syndrome and other forms of inherited thoracic aortic aneurysm taking ccbs display increased risk of aortic dissection and need for aortic surgery, compared to patients on other antihypertensive agents.
PubMedID- 22664289 Subclavian artery aneurysm in marfan syndrome.
PubMedID- 20150820 Objectives: the aim of the study is to compare mid-term results of bentall aortic root replacement with composite mechanical valved conduit and aortic valve reimplantation procedure using the valsalva graft for the treatment of aortic root aneurysm in patients with marfan syndrome.

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