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2,832 Possible Causes for Marfan Syndrome

  • Aortic Aneurysm and Dissection

    syndrome (MFS).[] Abstract In the current article, 3 cases of aortic aneurysm and dissection in pregnant patients with Marfan's syndrome are reported.[] Large aortic aneurysm and dissection in a patient with Marfan's syndrome Abstract Marfan’s syndrome is an autosomal dominant disorder of connective tissue affecting approximately1[]

  • Marfan Syndrome

    Reviewed February 2008 What is Marfan syndrome? Marfan syndrome is a disorder of the connective tissue.[] Is there a test for Marfan syndrome? There is no single test for Marfan syndrome.[] The incidence of Marfan syndrome is approximately 1 in 5,000 worldwide. Mutations in the FBN1 gene cause Marfan syndrome.[]

  • Mitral Valve Prolapse

    KEYWORDS: Marfan syndrome; mitral valve prolapse[] Mitral valve prolapse (MVP) is a common pathological finding in several inherited connective-tissue diseases among which the Marfan syndrome.[] We describe the case of a 3-year-old child with neonatal Marfan syndrome complicated by mitral valve prolapse with regurgitation, marked aortic root dilatation, and ventricular[]

  • Osteogenesis Imperfecta

    In this review we document that only very few CAD patients are affected by known inherited connective tissue disorders like Ehlers-Danlos syndrome, Marfan syndrome or Osteogenesis[] Marsalese DL, Moodie DS, Lytle BW et al (1990) Cystic medial necrosis of the aorta in patients without Marfan's syndrome: surgical outcome and long-term follow-up.[] syndrome with cardiovascular anomaly BKD Gupta, RK Basu The British Journal of Ophthalmology 39 (9), 566 , 1955 8 1955 Leptospirosis in India BMD Gupta The Indian Medical[]

  • Thoracic Aortic Aneurysm

    Comparative survival and predictors of outcomes in nonsyndromic TAA (NS-TAA) are incompletely defined compared to Marfan syndrome (MFS) and bicuspid aortic valve (BAV).[] Our center also participates in the International Registry of Acute Aortic Dissection and the Valve-Sparing Aortic Root Replacement Registry in Marfan Syndrome.[] Marfan syndrome and related disorders.[]

  • Rare Disease with Thoracic Aortic Aneurysm and Aortic Dissection

    In most cases, Marfan syndrome is inherited.[] Marfan syndrome Marfan syndrome, characterized by otosomal dominant inheritance, I was first described in 1986.[] This disorder can occur as nonsyndromic TAAD or in conjunction with other genetic syndromes including Marfan syndrome, Loeys-Dietz syndrome, Ehlers-Danolos, and other related[]

  • Aortic Dissection

    He did not have a Marfan syndrome (MFS)-like appearance, and had a history of a type B aortic dissection and total arch replacement.[] Abstract The Marfan syndrome is a dominantly inherited disorder of connective tissue with multisystem involvement.[] This poor survival was demonstrated in a series of 257 patients with the Marfan syndrome. The average age at death for the 72 deceased patients was 32 years.[]

  • Aortic Valve Insufficiency

    It may also occur in Marfan's syndrome, Ehlers-Danlos syndrome type IV and Turner syndrome.[] Such abnormalities may occur with the following conditions: Longstanding, uncontrolled hypertension Marfan syndrome Idiopathic aortic dilation Cystic medial necrosis Senile[] In patients with a dilated aorta, especially in patients with Marfan's syndrome or with a bicuspid valve, echocardiography should be performed on a yearly basis.[]

  • Aortic Aneurysm

    Marfan syndrome and related disorders.[] Sometimes people with inherited connective tissue disorders, such as Marfan syndrome and Ehlers-Danlos syndrome, get thoracic aortic aneurysms.[] We present the case of a 56-year-old man with Marfan syndrome, suffering abdominal aortic aneurysm (AAA) enlargement from a type Ib endoleak after previous EVAR with 2 Endofit[]

  • Multiple Endocrine Neoplasia Type 2B

    syndrome and multiple endocrine neoplasia type 2B.[] Dural ectasia can be seen in anchylosing spondylitis, achondroplasia, Loeys-Dietz syndrome and in the vascular form of Ehlers-Danlos syndrome besides Marfan syndrome.[] MEN 2 B is characterized by medullary thyroid carcinoma, pheochromocytomas, mucosal neuromas, ganglioneuromas of the intestinal tract, and Marfan's syndrome.[]

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