enow.com Web Search

  1. Ad

    related to: aortic anomaly genetic disorders symptoms
  2. wexnermedical.osu.edu has been visited by 10K+ users in the past month

Search results

  1. Results from the WOW.Com Content Network
  2. Aortic arch anomaly - peculiar facies - intellectual disability

    en.wikipedia.org/wiki/Aortic_arch_anomaly...

    This disorder was first discovered in 1968, [4] when a mother and 3 of her children (4 cases) were described with the symptoms mentioned above. In this case, additional features were found in a majority of the patients; three of the patients had esophageal indentation and left ligamentum arteriosum, two of the patients, a still-born baby, had anencephaly.

  3. Familial thoracic aortic aneurysm and aortic dissection

    en.wikipedia.org/wiki/Familial_thoracic_aortic...

    [1] [2] This disorder is the cause of 20% of thoracic aortic aneurysms [3] [4] Some families affected by this condition have shown mild versions of some symptoms that are associated with Marfan syndrome and Loeys-Dietz syndrome , these signs include tall stature, joint hypermobility , cutaneous stretch marks , and either pectus excavatum or ...

  4. Familial aortic dissection - Wikipedia

    en.wikipedia.org/wiki/Familial_aortic_dissection

    Familial aortic dissection or FAD refers to the splitting of the wall of the aorta in either the arch, ascending or descending portions. FAD is thought to be passed down as an autosomal dominant disease and once inherited will result in dissection of the aorta, and dissecting aneurysm of the aorta, or rarely aortic or arterial dilation at a young age.

  5. Marfan syndrome - Wikipedia

    en.wikipedia.org/wiki/Marfan_syndrome

    Marfan syndrome (MFS) is a multi-systemic genetic disorder that affects the connective tissue. [6] [7] [1] Those with the condition tend to be tall and thin, with long arms, legs, fingers, and toes. [1]

  6. Supravalvular aortic stenosis - Wikipedia

    en.wikipedia.org/wiki/Supravalvular_aortic_stenosis

    Supravalvular aortic stenosis is a congenital obstructive narrowing of the aorta just above the aortic valve and is the least common type of aortic stenosis. It is often associated with other cardiovascular anomalies and is one of the characteristic findings of Williams syndrome. The diagnosis can be made by echocardiography or MRI.

  7. Interrupted aortic arch - Wikipedia

    en.wikipedia.org/wiki/Interrupted_aortic_arch

    Type B: The aortic arch is interrupted between the left common carotid artery and the left subclavian artery. This is the most common form of the condition, and is the classification most often associated with DiGeorge syndrome. [2] [5] Type C: The aortic arch is interrupted between the innominate artery and the left common carotid artery. This ...

  8. Congenital contractural arachnodactyly - Wikipedia

    en.wikipedia.org/wiki/Congenital_contractural_ar...

    Congenital contractural arachnodactyly (CCA), also known as Beals–Hecht syndrome, is a rare autosomal dominant congenital connective tissue disorder. [1] As with Marfan syndrome , people with CCA typically have an arm span that is greater than their height and very long fingers and toes . [ 2 ]

  9. Congenital heart defect - Wikipedia

    en.wikipedia.org/wiki/Congenital_heart_defect

    A congenital heart defect is classed as a cardiovascular disease. [10] Signs and symptoms depend on the specific type of defect. [3] Symptoms can vary from none to life-threatening. [7] When present, symptoms are variable and may include rapid breathing, bluish skin , poor weight gain, and feeling tired. [2] CHD does not cause chest pain. [2]

  1. Ad

    related to: aortic anomaly genetic disorders symptoms