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  2. 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 ]

  3. Expressivity (genetics) - Wikipedia

    en.wikipedia.org/wiki/Expressivity_(genetics)

    Individuals with Marfan Syndrome usually have fingers that are longer than those that do not have the syndrome. The extremity of difference in finger length is a result of variable expressivity. Some common syndromes that involved phenotypic variability due to expressivity include: Marfan syndrome, Van der Woude Syndrome, and neurofibromatosis.

  4. Genetic disorder - Wikipedia

    en.wikipedia.org/wiki/Genetic_disorder

    A genetic disorder is a health problem caused by one or more abnormalities in the genome. ... Marfan syndrome: 1 in 4,000 [14] Huntington's disease: 1 in 15,000 [15]

  5. Familial thoracic aortic aneurysm - Wikipedia

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

    2 Genetics. 3 Diagnosis. 4 Treatment. 5 ... There is an association between familial thoracic aortic aneurysm and Marfan syndrome as well as other hereditary ...

  6. Arachnodactyly - Wikipedia

    en.wikipedia.org/wiki/Arachnodactyly

    It remains unconfirmed whether composer Sergei Rachmaninoff's abnormally large reach on a piano was a result of arachnodactyly due to Marfan syndrome, as the pianist exhibited no other signs of the disease. [6]

  7. Chromosome 15 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_15

    Prader-Willi syndrome is caused by the loss of active genes in a specific part of chromosome 15, the 15q11-q13 region. People normally have two copies of this chromosome in each cell, one copy from each parent. Prader–Willi syndrome occurs when the paternal copy is partly or entirely missing.

  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. 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]