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  2. Marfan syndrome - Wikipedia

    en.wikipedia.org/wiki/Marfan_syndrome

    Marfan syndrome is treated by addressing each issue as it arises and, in particular, preventive medication even for young children to slow progression of aortic dilation. The goal of this treatment strategy is to slow the progression of aortic dilation and prevent any damage to heart valves by eliminating heart arrhythmias , minimizing the ...

  3. Dural ectasia - Wikipedia

    en.wikipedia.org/wiki/Dural_ectasia

    Dural ectasia is common in Marfan syndrome, [3] occurring in 63–92% of people with the syndrome. [11] It may also occur in Ehlers-Danlos Syndrome , neurofibromatosis type I , [ 12 ] ankylosing spondylitis , [ 1 ] and is associated with spondylolisthesis , vertebral fractures, [ 13 ] scoliosis , tumors or trauma .

  4. He didn't know his aorta was about to burst. His son's rare ...

    www.aol.com/news/didnt-know-aorta-burst-sons...

    What is Marfan syndrome? This genetic disorder of the connective tissue impacts heart health. Causes long bones. People have long arms, legs.

  5. Cerebrospinal fluid leak - Wikipedia

    en.wikipedia.org/wiki/Cerebrospinal_fluid_leak

    [24] [43] Marfan syndrome, Ehlers–Danlos syndrome, and autosomal dominant polycystic kidney disease are the three most common connective tissue disorders associated with sCSFLs. [24] Roughly 20% of patients with a sCSFL exhibit features of Marfan syndrome, including tall stature, hollowed chest ( pectus excavatum ), joint hypermobility and ...

  6. 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]

  7. Sudden cardiac death of athletes - Wikipedia

    en.wikipedia.org/wiki/Sudden_cardiac_death_of...

    Heritable connective tissue diseases are rare, each disorder estimated at one to ten per 100,000, of which Marfan syndrome is the most common. It is carried by the FBN1 gene on chromosome 15, which encodes the connective protein fibrillin-1, [ 12 ] [ 13 ] inherited as a dominant trait.

  8. Congenital heart defect - Wikipedia

    en.wikipedia.org/wiki/Congenital_heart_defect

    A number of genetic conditions are associated with heart defects, including Down syndrome, Turner syndrome, and Marfan syndrome. [3] Congenital heart defects are divided into two main groups: cyanotic heart defects and non-cyanotic heart defects, depending on whether the child has the potential to turn bluish in color. [3]

  9. How did John Ritter die? Wife revisits his misdiagnosed heart ...

    www.aol.com/news/did-john-ritter-die-wife...

    Ritter's official cause of death was an undetected aortic dissection, when the body's main artery, aka the aorta, tears. However, doctors initially thought the actor was experiencing a heart attack.